Canonical Allele Identifier: CA1467373272

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756912_71756913delinsCA , CM000666.2:g.71756912_71756913delinsCA	GRCh38
NC_000004.11:g.72622629_72622630delinsCA , CM000666.1:g.72622629_72622630delinsCA	GRCh37
NC_000004.10:g.72841493_72841494delinsCA	NCBI36
NG_012837.2:g.53608_53609delinsTG
NG_012837.3:g.53608_53609delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.833_834delinsTG MANE Select	ENSP00000273951.8:p.Leu278=
ENST00000273951.12:c.833_834delinsTG	ENSP00000273951.8:p.Leu278=
ENST00000503472.5:n.717_718delinsTG
ENST00000504199.5:c.890_891delinsTG	ENSP00000421725.1:p.Leu297=
ENST00000509740.5:c.833_834delinsTG	ENSP00000422664.1:p.Leu278=
ENST00000513476.5:c.833_834delinsTG	ENSP00000426683.1:p.Leu278=
NM_000583.3:c.833_834delinsTG	NP_000574.2:p.Leu278=
NM_001204306.1:c.833_834delinsTG	NP_001191235.1:p.Leu278=
NM_001204307.1:c.890_891delinsTG	NP_001191236.1:p.Leu297=
XM_006714177.2:c.833_834delinsTG	XP_006714240.1:p.Leu278=
XM_006714177.3:c.833_834delinsTG	XP_006714240.1:p.Leu278=
NM_000583.4:c.833_834delinsTG MANE Select	NP_000574.2:p.Leu278=