Canonical Allele Identifier: CA1286884448

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428397C= , CM000664.2:g.127428397C=	GRCh38
NC_000002.11:g.128185973C= , CM000664.1:g.128185973C=	GRCh37
NC_000002.10:g.127902443C=	NCBI36
NG_016323.1:g.14978C= , LRG_599:g.14978C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.837C= MANE Select	ENSP00000234071.4:p.Asp279=
ENST00000234071.7:c.837C=	ENSP00000234071.3:p.Asp279=
ENST00000402125.2:c.161C=
ENST00000409048.1:c.939C=	ENSP00000386679.1:p.Asp313=
NM_000312.3:c.837C= , LRG_599t1:c.837C=	NP_000303.1:p.Asp279=
XM_005263715.3:c.1020C=	XP_005263772.1:p.Asp340=
XM_005263716.3:c.1002C=	XP_005263773.1:p.Asp334=
XM_005263717.3:c.900C=	XP_005263774.1:p.Asp300=
XR_923313.1:n.1332-133G=
XM_005263717.4:c.900C=	XP_005263774.1:p.Asp300=
XM_017004505.1:c.1080C=	XP_016859994.1:p.Asp360=
XM_024453002.1:c.1182C=	XP_024308770.1:p.Asp394=
XM_024453003.1:c.1122C=	XP_024308771.1:p.Asp374=
XM_024453004.1:c.1020C=	XP_024308772.1:p.Asp340=
XM_024453005.1:c.1002C=	XP_024308773.1:p.Asp334=
XM_024453006.1:c.939C=	XP_024308774.1:p.Asp313=
XR_001739705.1:n.3607-133G=
XR_923313.2:n.4043-133G=
NM_000312.4:c.837C= MANE Select	NP_000303.1:p.Asp279=
NM_001375602.1:c.1020C=	NP_001362531.1:p.Asp340=
NM_001375603.1:c.1002C=	NP_001362532.1:p.Asp334=
NM_001375604.1:c.900C=	NP_001362533.1:p.Asp300=
NM_001375605.1:c.939C=	NP_001362534.1:p.Asp313=
NM_001375606.1:c.1005C=	NP_001362535.1:p.Asp335=
NM_001375607.1:c.1023C=	NP_001362536.1:p.Asp341=
NM_001375608.1:c.780C=	NP_001362537.1:p.Asp260=
NM_001375609.1:c.813C=	NP_001362538.1:p.Asp271=
NM_001375610.1:c.831C=	NP_001362539.1:p.Asp277=
NM_001375611.1:c.837C=	NP_001362540.1:p.Asp279=
NM_001375613.1:c.837C=	NP_001362542.1:p.Asp279=