Canonical Allele Identifier: CA1467372781

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71755810_71755812delinsTTA , CM000666.2:g.71755810_71755812delinsTTA	GRCh38
NC_000004.11:g.72621527_72621529delinsTTA , CM000666.1:g.72621527_72621529delinsTTA	GRCh37
NC_000004.10:g.72840391_72840393delinsTTA	NCBI36
NG_012837.2:g.54709_54711delinsTAA
NG_012837.3:g.54709_54711delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.1035-705_1035-703delinsTAA MANE Select	ENSP00000273951.8:n.1035-705_1035-703delinsTAA
ENST00000273951.12:c.1035-705_1035-703delinsTAA	ENSP00000273951.8:n.1035-705_1035-703delinsTAA
ENST00000503472.5:n.919-705_919-703delinsTAA
ENST00000504199.5:c.1092-705_1092-703delinsTAA	ENSP00000421725.1:n.1092-705_1092-703delinsTAA
ENST00000509740.5:c.1034+900_1034+902delinsTAA	ENSP00000422664.1:n.1034+900_1034+902delinsTAA
ENST00000513476.5:c.1035-705_1035-703delinsTAA	ENSP00000426683.1:n.1035-705_1035-703delinsTAA
NM_000583.3:c.1035-705_1035-703delinsTAA	NP_000574.2:n.1035-705_1035-703delinsTAA
NM_001204306.1:c.1035-705_1035-703delinsTAA	NP_001191235.1:n.1035-705_1035-703delinsTAA
NM_001204307.1:c.1092-705_1092-703delinsTAA	NP_001191236.1:n.1092-705_1092-703delinsTAA
XM_006714177.2:c.1035-705_1035-703delinsTAA	XP_006714240.1:n.1035-705_1035-703delinsTAA
XM_006714177.3:c.1035-705_1035-703delinsTAA	XP_006714240.1:n.1035-705_1035-703delinsTAA
NM_000583.4:c.1035-705_1035-703delinsTAA MANE Select	NP_000574.2:n.1035-705_1035-703delinsTAA