Canonical Allele Identifier: CA2634920470

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89145411-CGGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145412_89145414del , CM000678.2:g.89145412_89145414del	GRCh38
NC_000016.9:g.89211820_89211822del , CM000678.1:g.89211820_89211822del	GRCh37
NC_000016.8:g.87739321_87739323del	NCBI36
NG_031961.1:g.56604_56606del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1501+11_1501+13del	ENSP00000320646.4:n.1501+11_1501+13del
ENST00000614302.5:c.1501+11_1501+13del MANE Select	ENSP00000479130.1:n.1501+11_1501+13del
ENST00000649953.1:c.1711+11_1711+13del	ENSP00000497456.1:n.1711+11_1711+13del
ENST00000317447.8:c.1501+11_1501+13del	ENSP00000320646.4:n.1501+11_1501+13del
ENST00000378345.8:c.706+11_706+13del	ENSP00000367596.4:n.706+11_706+13del
ENST00000406948.7:c.1501+11_1501+13del	ENSP00000384627.3:n.1501+11_1501+13del
ENST00000537116.5:n.627+11_627+13del
ENST00000537155.1:n.241+11_241+13del
ENST00000542688.5:c.*245+11_*245+13del	ENSP00000446281.1:n.*245+11_*245+13del
ENST00000562204.1:n.474+11_474+13del
ENST00000614302.4:c.1501+11_1501+13del	ENSP00000479130.1:n.1501+11_1501+13del
NM_001127214.3:c.1501+11_1501+13del	NP_001120686.1:n.1501+11_1501+13del
NM_001243279.2:c.1501+11_1501+13del	NP_001230208.1:n.1501+11_1501+13del
NM_001284316.1:c.706+11_706+13del	NP_001271245.1:n.706+11_706+13del
NM_174917.4:c.1501+11_1501+13del	NP_777577.2:n.1501+11_1501+13del
NR_045667.2:n.627+11_627+13del
NR_104293.1:n.1935+11_1935+13del
XM_005256293.1:c.1501+11_1501+13del	XP_005256350.1:n.1501+11_1501+13del
XM_011522942.1:c.1501+11_1501+13del	XP_011521244.1:n.1501+11_1501+13del
XM_011522943.1:c.1501+11_1501+13del	XP_011521245.1:n.1501+11_1501+13del
XR_933239.1:n.1942+11_1942+13del
XR_933240.1:n.1939+11_1939+13del
XR_933241.1:n.1696+11_1696+13del
NR_147928.1:n.1979+11_1979+13del
NR_147929.1:n.1733+11_1733+13del
XM_005256293.2:c.1501+11_1501+13del	XP_005256350.1:n.1501+11_1501+13del
XM_017023018.1:c.1501+11_1501+13del	XP_016878507.1:n.1501+11_1501+13del
XM_017023019.1:c.1501+11_1501+13del	XP_016878508.1:n.1501+11_1501+13del
XM_017023020.2:c.-3604+11_-3604+13del	XP_016878509.1:n.-3604+11_-3604+13del
XM_017023022.1:c.634+11_634+13del	XP_016878511.1:n.634+11_634+13del
XM_024450186.1:c.706+11_706+13del	XP_024305954.1:n.706+11_706+13del
XM_024450187.1:c.706+11_706+13del	XP_024305955.1:n.706+11_706+13del
XR_001751864.2:n.1748+11_1748+13del
XR_001751865.1:n.1695+11_1695+13del
XR_933240.3:n.1938+11_1938+13del
NM_001127214.4:c.1501+11_1501+13del	NP_001120686.1:n.1501+11_1501+13del
NM_001243279.3:c.1501+11_1501+13del MANE Select	NP_001230208.1:n.1501+11_1501+13del
NM_001284316.2:c.706+11_706+13del	NP_001271245.1:n.706+11_706+13del
NM_174917.5:c.1501+11_1501+13del	NP_777577.2:n.1501+11_1501+13del
NR_104293.2:n.1892+11_1892+13del
NR_147928.2:n.1936+11_1936+13del
NR_147929.2:n.1690+11_1690+13del