Canonical Allele Identifier: CA1240221376

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27322258_27322259delinsAC , CM000664.2:g.27322258_27322259delinsAC	GRCh38
NC_000002.11:g.27545125_27545126delinsAC , CM000664.1:g.27545125_27545126delinsAC	GRCh37
NC_000002.10:g.27398629_27398630delinsAC	NCBI36
NG_008075.1:g.5306_5307delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.70+189_70+190delinsGT MANE Select	ENSP00000369383.1:n.70+189_70+190delinsGT
ENST00000233545.6:c.70+189_70+190delinsGT	ENSP00000233545.2:n.70+189_70+190delinsGT
ENST00000357186.10:c.18+2174_18+2175delinsGT	ENSP00000349713.6:n.18+2174_18+2175delinsGT
ENST00000380044.5:c.70+189_70+190delinsGT	ENSP00000369383.1:n.70+189_70+190delinsGT
ENST00000399052.8:c.70+189_70+190delinsGT	ENSP00000382006.4:n.70+189_70+190delinsGT
ENST00000402310.5:c.70+189_70+190delinsGT	ENSP00000383955.1:n.70+189_70+190delinsGT
ENST00000402722.5:c.70+189_70+190delinsGT	ENSP00000386000.1:n.70+189_70+190delinsGT
ENST00000403262.6:c.70+189_70+190delinsGT	ENSP00000385671.1:n.70+189_70+190delinsGT
ENST00000405076.5:c.70+189_70+190delinsGT	ENSP00000385175.1:n.70+189_70+190delinsGT
ENST00000405983.5:c.70+189_70+190delinsGT	ENSP00000384586.1:n.70+189_70+190delinsGT
ENST00000415514.5:c.70+189_70+190delinsGT	ENSP00000388043.1:n.70+189_70+190delinsGT
ENST00000426513.6:c.70+189_70+190delinsGT	ENSP00000403824.2:n.70+189_70+190delinsGT
ENST00000428910.5:c.-133+189_-133+190delinsGT	ENSP00000405235.1:n.-133+189_-133+190delinsGT
ENST00000486898.1:n.121+189_121+190delinsGT
ENST00000494436.1:n.290_291delinsGT
ENST00000617583.4:n.96+189_96+190delinsGT
ENST00000621183.4:n.126+189_126+190delinsGT
ENST00000621470.4:n.121+189_121+190delinsGT
ENST00000622003.4:n.86+189_86+190delinsGT
NM_002437.4:c.70+189_70+190delinsGT	NP_002428.1:n.70+189_70+190delinsGT
XM_005264326.2:c.70+189_70+190delinsGT	XP_005264383.1:n.70+189_70+190delinsGT
XM_005264327.2:c.-55+189_-55+190delinsGT	XP_005264384.1:n.-55+189_-55+190delinsGT
XM_006712021.2:c.-136+189_-136+190delinsGT	XP_006712084.1:n.-136+189_-136+190delinsGT
XM_005264326.4:c.70+189_70+190delinsGT	XP_005264383.1:n.70+189_70+190delinsGT
XM_006712021.3:c.-136+189_-136+190delinsGT	XP_006712084.1:n.-136+189_-136+190delinsGT
XM_017004150.1:c.-3183+189_-3183+190delinsGT	XP_016859639.1:n.-3183+189_-3183+190delinsGT
XM_017004151.1:c.-75+189_-75+190delinsGT	XP_016859640.1:n.-75+189_-75+190delinsGT
XM_017004152.1:c.-212+189_-212+190delinsGT	XP_016859641.1:n.-212+189_-212+190delinsGT
XM_024452913.1:c.-136+189_-136+190delinsGT	XP_024308681.1:n.-136+189_-136+190delinsGT
NM_002437.5:c.70+189_70+190delinsGT MANE Select	NP_002428.1:n.70+189_70+190delinsGT