Canonical Allele Identifier: CA1286880853

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127421374C= , CM000664.2:g.127421374C=	GRCh38
NC_000002.11:g.128178950C= , CM000664.1:g.128178950C=	GRCh37
NC_000002.10:g.127895420C=	NCBI36
NG_016323.1:g.7955C= , LRG_599:g.7955C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.162C= MANE Select	ENSP00000234071.4:p.Ser54=
ENST00000234071.7:c.162C=	ENSP00000234071.3:p.Ser54=
ENST00000409048.1:c.162C=	ENSP00000386679.1:p.Ser54=
ENST00000419985.5:c.127C=	ENSP00000392606.1:p.Pro43=
ENST00000427769.5:c.162C=	ENSP00000406295.1:p.Ser54=
ENST00000429925.5:c.162C=	ENSP00000412697.1:p.Ser54=
ENST00000431364.1:c.127C=	ENSP00000391220.1:p.Pro43=
ENST00000442644.5:c.162C=	ENSP00000411241.1:p.Ser54=
ENST00000474030.5:n.245C=
NM_000312.3:c.162C= , LRG_599t1:c.162C=	NP_000303.1:p.Ser54=
XM_005263715.3:c.345C=	XP_005263772.1:p.Ser115=
XM_005263716.3:c.225C=	XP_005263773.1:p.Ser75=
XM_005263717.3:c.225C=	XP_005263774.1:p.Ser75=
XM_005263717.4:c.225C=	XP_005263774.1:p.Ser75=
XM_017004505.1:c.405C=	XP_016859994.1:p.Ser135=
XM_024453002.1:c.405C=	XP_024308770.1:p.Ser135=
XM_024453003.1:c.345C=	XP_024308771.1:p.Ser115=
XM_024453004.1:c.345C=	XP_024308772.1:p.Ser115=
XM_024453005.1:c.225C=	XP_024308773.1:p.Ser75=
XM_024453006.1:c.162C=	XP_024308774.1:p.Ser54=
NM_000312.4:c.162C= MANE Select	NP_000303.1:p.Ser54=
NM_001375602.1:c.345C=	NP_001362531.1:p.Ser115=
NM_001375603.1:c.225C=	NP_001362532.1:p.Ser75=
NM_001375604.1:c.225C=	NP_001362533.1:p.Ser75=
NM_001375605.1:c.162C=	NP_001362534.1:p.Ser54=
NM_001375606.1:c.225C=	NP_001362535.1:p.Ser75=
NM_001375607.1:c.246C=	NP_001362536.1:p.Ser82=
NM_001375608.1:c.162C=	NP_001362537.1:p.Ser54=
NM_001375609.1:c.138C=	NP_001362538.1:p.Ser46=
NM_001375610.1:c.156C=	NP_001362539.1:p.Ser52=
NM_001375611.1:c.162C=	NP_001362540.1:p.Ser54=
NM_001375613.1:c.162C=	NP_001362542.1:p.Ser54=