Canonical Allele Identifier: CA1286884696

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428878C= , CM000664.2:g.127428878C=	GRCh38
NC_000002.11:g.128186454C= , CM000664.1:g.128186454C=	GRCh37
NC_000002.10:g.127902924C=	NCBI36
NG_016323.1:g.15459C= , LRG_599:g.15459C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1318C= MANE Select	ENSP00000234071.4:p.Arg440=
ENST00000234071.7:c.1318C=	ENSP00000234071.3:p.Arg440=
ENST00000402125.2:c.642C=
ENST00000409048.1:c.1420C=	ENSP00000386679.1:p.Arg474=
NM_000312.3:c.1318C= , LRG_599t1:c.1318C=	NP_000303.1:p.Arg440=
XM_005263715.3:c.1501C=	XP_005263772.1:p.Arg501=
XM_005263716.3:c.1483C=	XP_005263773.1:p.Arg495=
XM_005263717.3:c.1381C=	XP_005263774.1:p.Arg461=
XR_923313.1:n.1332-614G=
XM_005263717.4:c.1381C=	XP_005263774.1:p.Arg461=
XM_017004505.1:c.1561C=	XP_016859994.1:p.Arg521=
XM_024453002.1:c.1663C=	XP_024308770.1:p.Arg555=
XM_024453003.1:c.1603C=	XP_024308771.1:p.Arg535=
XM_024453004.1:c.1501C=	XP_024308772.1:p.Arg501=
XM_024453005.1:c.1483C=	XP_024308773.1:p.Arg495=
XM_024453006.1:c.1420C=	XP_024308774.1:p.Arg474=
XR_001739705.1:n.3607-614G=
XR_923313.2:n.4043-614G=
NM_000312.4:c.1318C= MANE Select	NP_000303.1:p.Arg440=
NM_001375602.1:c.1501C=	NP_001362531.1:p.Arg501=
NM_001375603.1:c.1483C=	NP_001362532.1:p.Arg495=
NM_001375604.1:c.1381C=	NP_001362533.1:p.Arg461=
NM_001375605.1:c.1420C=	NP_001362534.1:p.Arg474=
NM_001375606.1:c.1486C=	NP_001362535.1:p.Arg496=
NM_001375607.1:c.1504C=	NP_001362536.1:p.Arg502=
NM_001375608.1:c.1261C=	NP_001362537.1:p.Arg421=
NM_001375609.1:c.1294C=	NP_001362538.1:p.Arg432=
NM_001375610.1:c.1312C=	NP_001362539.1:p.Arg438=
NM_001375611.1:c.1318C=	NP_001362540.1:p.Arg440=
NM_001375613.1:c.1318C=	NP_001362542.1:p.Arg440=