Canonical Allele Identifier: CA1619028888

Gene: CCHCR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31157013_31157014delinsTC , CM000668.2:g.31157013_31157014delinsTC	GRCh38
NC_000006.11:g.31124790_31124791delinsTC , CM000668.1:g.31124790_31124791delinsTC	GRCh37
NC_000006.10:g.31232769_31232770delinsTC	NCBI36
NG_054878.1:g.6225_6226delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396268.8:c.283+9_283+10delinsGA MANE Select	ENSP00000379566.3:n.283+9_283+10delinsGA
ENST00000652427.1:c.16+9_16+10delinsGA	ENSP00000498342.1:n.16+9_16+10delinsGA
ENST00000652535.1:c.16+9_16+10delinsGA	ENSP00000498479.1:n.16+9_16+10delinsGA
ENST00000376266.9:c.16+9_16+10delinsGA	ENSP00000365442.5:n.16+9_16+10delinsGA
ENST00000396263.6:c.16+9_16+10delinsGA	ENSP00000379561.2:n.16+9_16+10delinsGA
ENST00000396268.7:c.283+9_283+10delinsGA	ENSP00000379566.3:n.283+9_283+10delinsGA
ENST00000426967.5:c.310+9_310+10delinsGA	ENSP00000402432.1:n.310+9_310+10delinsGA
ENST00000428174.1:c.25_26delinsGA	ENSP00000389303.1:p.Asp9=
ENST00000448141.6:c.16+9_16+10delinsGA	ENSP00000414323.2:n.16+9_16+10delinsGA
ENST00000448162.6:c.16+9_16+10delinsGA	ENSP00000390027.2:n.16+9_16+10delinsGA
ENST00000451521.6:c.283+9_283+10delinsGA	ENSP00000401039.2:n.283+9_283+10delinsGA
ENST00000455279.6:c.16+9_16+10delinsGA	ENSP00000398715.2:n.16+9_16+10delinsGA
ENST00000475684.2:n.73+9_73+10delinsGA
ENST00000480060.5:n.92+9_92+10delinsGA
ENST00000488920.2:c.*106+9_*106+10delinsGA	ENSP00000422000.1:n.*106+9_*106+10delinsGA
ENST00000502557.5:c.16+9_16+10delinsGA	ENSP00000425377.1:n.16+9_16+10delinsGA
ENST00000503420.5:c.16+9_16+10delinsGA	ENSP00000421992.1:n.16+9_16+10delinsGA
ENST00000503934.5:c.16+9_16+10delinsGA	ENSP00000425595.1:n.16+9_16+10delinsGA
ENST00000505392.5:n.95+9_95+10delinsGA
ENST00000506831.1:c.16+9_16+10delinsGA	ENSP00000425435.1:n.16+9_16+10delinsGA
ENST00000507226.1:c.16+9_16+10delinsGA	ENSP00000424335.1:n.16+9_16+10delinsGA
ENST00000507459.5:c.16+9_16+10delinsGA	ENSP00000421523.1:n.16+9_16+10delinsGA
ENST00000507751.5:c.16+9_16+10delinsGA	ENSP00000420941.1:n.16+9_16+10delinsGA
ENST00000507829.5:c.16+9_16+10delinsGA	ENSP00000420911.1:n.16+9_16+10delinsGA
ENST00000507892.1:c.16+9_16+10delinsGA	ENSP00000424164.1:n.16+9_16+10delinsGA
ENST00000508683.5:c.16+9_16+10delinsGA	ENSP00000421393.1:n.16+9_16+10delinsGA
ENST00000508852.5:c.16+9_16+10delinsGA	ENSP00000422503.1:n.16+9_16+10delinsGA
ENST00000509552.5:n.157+9_157+10delinsGA
ENST00000512418.5:c.16+9_16+10delinsGA	ENSP00000426883.1:n.16+9_16+10delinsGA
ENST00000513222.1:c.-62-70_-62-69delinsGA	ENSP00000425682.1:n.-62-70_-62-69delinsGA
NM_001105563.1:c.283+9_283+10delinsGA	NP_001099033.1:n.283+9_283+10delinsGA
NM_001105564.1:c.283+9_283+10delinsGA	NP_001099034.1:n.283+9_283+10delinsGA
NM_019052.3:c.16+9_16+10delinsGA	NP_061925.2:n.16+9_16+10delinsGA
XM_011514702.1:c.310+9_310+10delinsGA	XP_011513004.1:n.310+9_310+10delinsGA
XM_011514703.1:c.16+9_16+10delinsGA	XP_011513005.1:n.16+9_16+10delinsGA
XM_011514704.1:c.16+9_16+10delinsGA	XP_011513006.1:n.16+9_16+10delinsGA
XM_011514705.1:c.16+9_16+10delinsGA	XP_011513007.1:n.16+9_16+10delinsGA
XM_011514706.1:c.16+9_16+10delinsGA	XP_011513008.1:n.16+9_16+10delinsGA
XM_011514702.2:c.310+9_310+10delinsGA	XP_011513004.1:n.310+9_310+10delinsGA
XM_011514704.3:c.16+9_16+10delinsGA	XP_011513006.1:n.16+9_16+10delinsGA
XM_017010961.1:c.310+9_310+10delinsGA	XP_016866450.1:n.310+9_310+10delinsGA
XM_017010962.2:c.16+9_16+10delinsGA	XP_016866451.1:n.16+9_16+10delinsGA
XM_017010963.1:c.16+9_16+10delinsGA	XP_016866452.1:n.16+9_16+10delinsGA
XM_017010964.1:c.16+9_16+10delinsGA	XP_016866453.1:n.16+9_16+10delinsGA
XM_017010965.1:c.16+9_16+10delinsGA	XP_016866454.1:n.16+9_16+10delinsGA
XM_017010966.1:c.16+9_16+10delinsGA	XP_016866455.1:n.16+9_16+10delinsGA
XM_017010967.1:c.16+9_16+10delinsGA	XP_016866456.1:n.16+9_16+10delinsGA
XM_017010968.1:c.16+9_16+10delinsGA	XP_016866457.1:n.16+9_16+10delinsGA
XM_017010969.1:c.16+9_16+10delinsGA	XP_016866458.1:n.16+9_16+10delinsGA
XM_017010970.1:c.-509+9_-509+10delinsGA	XP_016866459.1:n.-509+9_-509+10delinsGA
XM_024446473.1:c.25_26delinsGA	XP_024302241.1:p.Asp9=
NM_019052.4:c.16+9_16+10delinsGA	NP_061925.2:n.16+9_16+10delinsGA
NM_001105563.2:c.283+9_283+10delinsGA	NP_001099033.1:n.283+9_283+10delinsGA
NM_001105563.3:c.283+9_283+10delinsGA	NP_001099033.1:n.283+9_283+10delinsGA
NM_001105564.2:c.283+9_283+10delinsGA MANE Select	NP_001099034.1:n.283+9_283+10delinsGA
NM_001394641.1:c.310+9_310+10delinsGA	NP_001381570.1:n.310+9_310+10delinsGA
NM_001394642.1:c.16+9_16+10delinsGA	NP_001381571.1:n.16+9_16+10delinsGA
NM_001394643.1:c.16+9_16+10delinsGA	NP_001381572.1:n.16+9_16+10delinsGA
NM_001394644.1:c.16+9_16+10delinsGA	NP_001381573.1:n.16+9_16+10delinsGA
NM_001394646.1:c.16+9_16+10delinsGA	NP_001381575.1:n.16+9_16+10delinsGA
NM_001394647.1:c.-62-70_-62-69delinsGA	NP_001381576.1:n.-62-70_-62-69delinsGA
NM_001394648.1:c.16+9_16+10delinsGA	NP_001381577.1:n.16+9_16+10delinsGA
NM_001394649.1:c.-128+1153_-128+1154delinsGA	NP_001381578.1:n.-128+1153_-128+1154delinsGA