Canonical Allele Identifier: CA1467372769

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71755791_71755792delinsGT , CM000666.2:g.71755791_71755792delinsGT	GRCh38
NC_000004.11:g.72621508_72621509delinsGT , CM000666.1:g.72621508_72621509delinsGT	GRCh37
NC_000004.10:g.72840372_72840373delinsGT	NCBI36
NG_012837.2:g.54729_54730delinsAC
NG_012837.3:g.54729_54730delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.1035-685_1035-684delinsAC MANE Select	ENSP00000273951.8:n.1035-685_1035-684deli...
ENST00000273951.12:c.1035-685_1035-684delinsAC	ENSP00000273951.8:n.1035-685_1035-684deli...
ENST00000503472.5:n.919-685_919-684delinsAC
ENST00000504199.5:c.1092-685_1092-684delinsAC	ENSP00000421725.1:n.1092-685_1092-684deli...
ENST00000509740.5:c.1034+920_1034+921delinsAC	ENSP00000422664.1:n.1034+920_1034+921deli...
ENST00000513476.5:c.1035-685_1035-684delinsAC	ENSP00000426683.1:n.1035-685_1035-684deli...
NM_000583.3:c.1035-685_1035-684delinsAC	NP_000574.2:n.1035-685_1035-684delinsAC
NM_001204306.1:c.1035-685_1035-684delinsAC	NP_001191235.1:n.1035-685_1035-684delinsA...
NM_001204307.1:c.1092-685_1092-684delinsAC	NP_001191236.1:n.1092-685_1092-684delinsA...
XM_006714177.2:c.1035-685_1035-684delinsAC	XP_006714240.1:n.1035-685_1035-684delinsA...
XM_006714177.3:c.1035-685_1035-684delinsAC	XP_006714240.1:n.1035-685_1035-684delinsA...
NM_000583.4:c.1035-685_1035-684delinsAC MANE Select	NP_000574.2:n.1035-685_1035-684delinsAC