Canonical Allele Identifier: CA1303182284

Gene: GCA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162352383T= , CM000664.2:g.162352383T=	GRCh38
NC_000002.11:g.163208893T= , CM000664.1:g.163208893T=	GRCh37
NC_000002.10:g.162917139T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437150.7:c.238T= MANE Select	ENSP00000394842.2:p.Ser80=
ENST00000233612.8:c.181T=	ENSP00000233612.4:p.Ser61=
ENST00000429691.6:c.181T=	ENSP00000412899.2:p.Ser61=
ENST00000437150.6:c.238T=	ENSP00000394842.2:p.Ser80=
ENST00000446271.5:c.316T=	ENSP00000393218.1:p.Ser106=
ENST00000453113.6:c.181T=	ENSP00000403805.2:p.Ser61=
ENST00000473240.5:n.669T=
ENST00000479199.1:n.305T=
ENST00000481161.5:n.353T=
ENST00000487445.6:n.328T=
NM_012198.3:c.238T=	NP_036330.1:p.Ser80=
XM_005246446.2:c.238T=	XP_005246503.1:p.Ser80=
XM_006712398.2:c.316T=	XP_006712461.1:p.Ser106=
XM_006712399.2:c.316T=	XP_006712462.1:p.Ser106=
XM_006712400.2:c.283T=	XP_006712463.1:p.Ser95=
XM_006712401.2:c.316T=	XP_006712464.1:p.Ser106=
XM_011510926.1:c.181T=	XP_011509228.1:p.Ser61=
XM_011510927.1:c.181T=	XP_011509229.1:p.Ser61=
NM_001330265.1:c.283T=	NP_001317194.1:p.Ser95=
NM_001330266.1:c.283T=	NP_001317195.1:p.Ser95=
NM_001330267.1:c.283T=	NP_001317196.1:p.Ser95=
NM_001330268.1:c.316T=	NP_001317197.1:p.Ser106=
NM_001330270.1:c.181T=	NP_001317199.1:p.Ser61=
NM_001330271.1:c.181T=	NP_001317200.1:p.Ser61=
NM_012198.4:c.238T=	NP_036330.1:p.Ser80=
XM_005246446.3:c.238T=	XP_005246503.1:p.Ser80=
XM_006712398.4:c.316T=	XP_006712461.1:p.Ser106=
XM_006712400.4:c.283T=	XP_006712463.1:p.Ser95=
XM_011510926.2:c.181T=	XP_011509228.1:p.Ser61=
XM_017003767.1:c.181T=	XP_016859256.1:p.Ser61=
XM_017003769.2:c.316T=	XP_016859258.1:p.Ser106=
NM_012198.5:c.238T= MANE Select	NP_036330.1:p.Ser80=
NM_001330270.2:c.181T=	NP_001317199.1:p.Ser61=
NM_001330271.2:c.181T=	NP_001317200.1:p.Ser61=