Canonical Allele Identifier: CA1286884651

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428789T= , CM000664.2:g.127428789T=	GRCh38
NC_000002.11:g.128186365T= , CM000664.1:g.128186365T=	GRCh37
NC_000002.10:g.127902835T=	NCBI36
NG_016323.1:g.15370T= , LRG_599:g.15370T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1229T= MANE Select	ENSP00000234071.4:p.Phe410=
ENST00000234071.7:c.1229T=	ENSP00000234071.3:p.Phe410=
ENST00000402125.2:c.553T=
ENST00000409048.1:c.1331T=	ENSP00000386679.1:p.Phe444=
NM_000312.3:c.1229T= , LRG_599t1:c.1229T=	NP_000303.1:p.Phe410=
XM_005263715.3:c.1412T=	XP_005263772.1:p.Phe471=
XM_005263716.3:c.1394T=	XP_005263773.1:p.Phe465=
XM_005263717.3:c.1292T=	XP_005263774.1:p.Phe431=
XR_923313.1:n.1332-525A=
XM_005263717.4:c.1292T=	XP_005263774.1:p.Phe431=
XM_017004505.1:c.1472T=	XP_016859994.1:p.Phe491=
XM_024453002.1:c.1574T=	XP_024308770.1:p.Phe525=
XM_024453003.1:c.1514T=	XP_024308771.1:p.Phe505=
XM_024453004.1:c.1412T=	XP_024308772.1:p.Phe471=
XM_024453005.1:c.1394T=	XP_024308773.1:p.Phe465=
XM_024453006.1:c.1331T=	XP_024308774.1:p.Phe444=
XR_001739705.1:n.3607-525A=
XR_923313.2:n.4043-525A=
NM_000312.4:c.1229T= MANE Select	NP_000303.1:p.Phe410=
NM_001375602.1:c.1412T=	NP_001362531.1:p.Phe471=
NM_001375603.1:c.1394T=	NP_001362532.1:p.Phe465=
NM_001375604.1:c.1292T=	NP_001362533.1:p.Phe431=
NM_001375605.1:c.1331T=	NP_001362534.1:p.Phe444=
NM_001375606.1:c.1397T=	NP_001362535.1:p.Phe466=
NM_001375607.1:c.1415T=	NP_001362536.1:p.Phe472=
NM_001375608.1:c.1172T=	NP_001362537.1:p.Phe391=
NM_001375609.1:c.1205T=	NP_001362538.1:p.Phe402=
NM_001375610.1:c.1223T=	NP_001362539.1:p.Phe408=
NM_001375611.1:c.1229T=	NP_001362540.1:p.Phe410=
NM_001375613.1:c.1229T=	NP_001362542.1:p.Phe410=