Canonical Allele Identifier: CA1286884635

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428760C= , CM000664.2:g.127428760C=	GRCh38
NC_000002.11:g.128186336C= , CM000664.1:g.128186336C=	GRCh37
NC_000002.10:g.127902806C=	NCBI36
NG_016323.1:g.15341C= , LRG_599:g.15341C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1200C= MANE Select	ENSP00000234071.4:p.Gly400=
ENST00000234071.7:c.1200C=	ENSP00000234071.3:p.Gly400=
ENST00000402125.2:c.524C=
ENST00000409048.1:c.1302C=	ENSP00000386679.1:p.Gly434=
NM_000312.3:c.1200C= , LRG_599t1:c.1200C=	NP_000303.1:p.Gly400=
XM_005263715.3:c.1383C=	XP_005263772.1:p.Gly461=
XM_005263716.3:c.1365C=	XP_005263773.1:p.Gly455=
XM_005263717.3:c.1263C=	XP_005263774.1:p.Gly421=
XR_923313.1:n.1332-496G=
XM_005263717.4:c.1263C=	XP_005263774.1:p.Gly421=
XM_017004505.1:c.1443C=	XP_016859994.1:p.Gly481=
XM_024453002.1:c.1545C=	XP_024308770.1:p.Gly515=
XM_024453003.1:c.1485C=	XP_024308771.1:p.Gly495=
XM_024453004.1:c.1383C=	XP_024308772.1:p.Gly461=
XM_024453005.1:c.1365C=	XP_024308773.1:p.Gly455=
XM_024453006.1:c.1302C=	XP_024308774.1:p.Gly434=
XR_001739705.1:n.3607-496G=
XR_923313.2:n.4043-496G=
NM_000312.4:c.1200C= MANE Select	NP_000303.1:p.Gly400=
NM_001375602.1:c.1383C=	NP_001362531.1:p.Gly461=
NM_001375603.1:c.1365C=	NP_001362532.1:p.Gly455=
NM_001375604.1:c.1263C=	NP_001362533.1:p.Gly421=
NM_001375605.1:c.1302C=	NP_001362534.1:p.Gly434=
NM_001375606.1:c.1368C=	NP_001362535.1:p.Gly456=
NM_001375607.1:c.1386C=	NP_001362536.1:p.Gly462=
NM_001375608.1:c.1143C=	NP_001362537.1:p.Gly381=
NM_001375609.1:c.1176C=	NP_001362538.1:p.Gly392=
NM_001375610.1:c.1194C=	NP_001362539.1:p.Gly398=
NM_001375611.1:c.1200C=	NP_001362540.1:p.Gly400=
NM_001375613.1:c.1200C=	NP_001362542.1:p.Gly400=