Canonical Allele Identifier: CA1467372860

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756012_71756013delinsCT , CM000666.2:g.71756012_71756013delinsCT	GRCh38
NC_000004.11:g.72621729_72621730delinsCT , CM000666.1:g.72621729_72621730delinsCT	GRCh37
NC_000004.10:g.72840593_72840594delinsCT	NCBI36
NG_012837.2:g.54508_54509delinsAG
NG_012837.3:g.54508_54509delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.1034+699_1034+700delinsAG MANE Select	ENSP00000273951.8:n.1034+699_1034+700deli...
ENST00000273951.12:c.1034+699_1034+700delinsAG	ENSP00000273951.8:n.1034+699_1034+700deli...
ENST00000503472.5:n.918+699_918+700delinsAG
ENST00000504199.5:c.1091+699_1091+700delinsAG	ENSP00000421725.1:n.1091+699_1091+700deli...
ENST00000509740.5:c.1034+699_1034+700delinsAG	ENSP00000422664.1:n.1034+699_1034+700deli...
ENST00000513476.5:c.1034+699_1034+700delinsAG	ENSP00000426683.1:n.1034+699_1034+700deli...
NM_000583.3:c.1034+699_1034+700delinsAG	NP_000574.2:n.1034+699_1034+700delinsAG
NM_001204306.1:c.1034+699_1034+700delinsAG	NP_001191235.1:n.1034+699_1034+700delinsA...
NM_001204307.1:c.1091+699_1091+700delinsAG	NP_001191236.1:n.1091+699_1091+700delinsA...
XM_006714177.2:c.1034+699_1034+700delinsAG	XP_006714240.1:n.1034+699_1034+700delinsA...
XM_006714177.3:c.1034+699_1034+700delinsAG	XP_006714240.1:n.1034+699_1034+700delinsA...
NM_000583.4:c.1034+699_1034+700delinsAG MANE Select	NP_000574.2:n.1034+699_1034+700delinsAG