Canonical Allele Identifier: CA1467372740

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71755738_71755740delinsACT , CM000666.2:g.71755738_71755740delinsACT	GRCh38
NC_000004.11:g.72621455_72621457delinsACT , CM000666.1:g.72621455_72621457delinsACT	GRCh37
NC_000004.10:g.72840319_72840321delinsACT	NCBI36
NG_012837.2:g.54781_54783delinsAGT
NG_012837.3:g.54781_54783delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.1035-633_1035-631delinsAGT MANE Select	ENSP00000273951.8:n.1035-633_1035-631delinsAGT
ENST00000273951.12:c.1035-633_1035-631delinsAGT	ENSP00000273951.8:n.1035-633_1035-631delinsAGT
ENST00000503472.5:n.919-633_919-631delinsAGT
ENST00000504199.5:c.1092-633_1092-631delinsAGT	ENSP00000421725.1:n.1092-633_1092-631delinsAGT
ENST00000509740.5:c.1034+972_1034+974delinsAGT	ENSP00000422664.1:n.1034+972_1034+974delinsAGT
ENST00000513476.5:c.1035-633_1035-631delinsAGT	ENSP00000426683.1:n.1035-633_1035-631delinsAGT
NM_000583.3:c.1035-633_1035-631delinsAGT	NP_000574.2:n.1035-633_1035-631delinsAGT
NM_001204306.1:c.1035-633_1035-631delinsAGT	NP_001191235.1:n.1035-633_1035-631delinsAGT
NM_001204307.1:c.1092-633_1092-631delinsAGT	NP_001191236.1:n.1092-633_1092-631delinsAGT
XM_006714177.2:c.1035-633_1035-631delinsAGT	XP_006714240.1:n.1035-633_1035-631delinsAGT
XM_006714177.3:c.1035-633_1035-631delinsAGT	XP_006714240.1:n.1035-633_1035-631delinsAGT
NM_000583.4:c.1035-633_1035-631delinsAGT MANE Select	NP_000574.2:n.1035-633_1035-631delinsAGT