Canonical Allele Identifier: CA1467372749

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71755749_71755750delinsAG , CM000666.2:g.71755749_71755750delinsAG	GRCh38
NC_000004.11:g.72621466_72621467delinsAG , CM000666.1:g.72621466_72621467delinsAG	GRCh37
NC_000004.10:g.72840330_72840331delinsAG	NCBI36
NG_012837.2:g.54771_54772delinsCT
NG_012837.3:g.54771_54772delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.1035-643_1035-642delinsCT MANE Select	ENSP00000273951.8:n.1035-643_1035-642delinsCT
ENST00000273951.12:c.1035-643_1035-642delinsCT	ENSP00000273951.8:n.1035-643_1035-642delinsCT
ENST00000503472.5:n.919-643_919-642delinsCT
ENST00000504199.5:c.1092-643_1092-642delinsCT	ENSP00000421725.1:n.1092-643_1092-642delinsCT
ENST00000509740.5:c.1034+962_1034+963delinsCT	ENSP00000422664.1:n.1034+962_1034+963delinsCT
ENST00000513476.5:c.1035-643_1035-642delinsCT	ENSP00000426683.1:n.1035-643_1035-642delinsCT
NM_000583.3:c.1035-643_1035-642delinsCT	NP_000574.2:n.1035-643_1035-642delinsCT
NM_001204306.1:c.1035-643_1035-642delinsCT	NP_001191235.1:n.1035-643_1035-642delinsCT
NM_001204307.1:c.1092-643_1092-642delinsCT	NP_001191236.1:n.1092-643_1092-642delinsCT
XM_006714177.2:c.1035-643_1035-642delinsCT	XP_006714240.1:n.1035-643_1035-642delinsCT
XM_006714177.3:c.1035-643_1035-642delinsCT	XP_006714240.1:n.1035-643_1035-642delinsCT
NM_000583.4:c.1035-643_1035-642delinsCT MANE Select	NP_000574.2:n.1035-643_1035-642delinsCT