Canonical Allele Identifier: CA1286884426

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428354C= , CM000664.2:g.127428354C=	GRCh38
NC_000002.11:g.128185930C= , CM000664.1:g.128185930C=	GRCh37
NC_000002.10:g.127902400C=	NCBI36
NG_016323.1:g.14935C= , LRG_599:g.14935C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.797-3C= MANE Select	ENSP00000234071.4:n.797-3C=
ENST00000234071.7:c.797-3C=	ENSP00000234071.3:n.797-3C=
ENST00000402125.2:c.121-3C=
ENST00000409048.1:c.899-3C=	ENSP00000386679.1:n.899-3C=
NM_000312.3:c.797-3C= , LRG_599t1:c.797-3C=	NP_000303.1:n.797-3C=
XM_005263715.3:c.980-3C=	XP_005263772.1:n.980-3C=
XM_005263716.3:c.962-3C=	XP_005263773.1:n.962-3C=
XM_005263717.3:c.860-3C=	XP_005263774.1:n.860-3C=
XR_923313.1:n.1332-90G=
XM_005263717.4:c.860-3C=	XP_005263774.1:n.860-3C=
XM_017004505.1:c.1040-3C=	XP_016859994.1:n.1040-3C=
XM_024453002.1:c.1142-3C=	XP_024308770.1:n.1142-3C=
XM_024453003.1:c.1082-3C=	XP_024308771.1:n.1082-3C=
XM_024453004.1:c.980-3C=	XP_024308772.1:n.980-3C=
XM_024453005.1:c.962-3C=	XP_024308773.1:n.962-3C=
XM_024453006.1:c.899-3C=	XP_024308774.1:n.899-3C=
XR_001739705.1:n.3607-90G=
XR_923313.2:n.4043-90G=
NM_000312.4:c.797-3C= MANE Select	NP_000303.1:n.797-3C=
NM_001375602.1:c.980-3C=	NP_001362531.1:n.980-3C=
NM_001375603.1:c.962-3C=	NP_001362532.1:n.962-3C=
NM_001375604.1:c.860-3C=	NP_001362533.1:n.860-3C=
NM_001375605.1:c.899-3C=	NP_001362534.1:n.899-3C=
NM_001375606.1:c.965-3C=	NP_001362535.1:n.965-3C=
NM_001375607.1:c.983-3C=	NP_001362536.1:n.983-3C=
NM_001375608.1:c.740-3C=	NP_001362537.1:n.740-3C=
NM_001375609.1:c.773-3C=	NP_001362538.1:n.773-3C=
NM_001375610.1:c.791-3C=	NP_001362539.1:n.791-3C=
NM_001375611.1:c.797-3C=	NP_001362540.1:n.797-3C=
NM_001375613.1:c.797-3C=	NP_001362542.1:n.797-3C=