Canonical Allele Identifier: CA1286884439

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428379G= , CM000664.2:g.127428379G=	GRCh38
NC_000002.11:g.128185955G= , CM000664.1:g.128185955G=	GRCh37
NC_000002.10:g.127902425G=	NCBI36
NG_016323.1:g.14960G= , LRG_599:g.14960G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.819G= MANE Select	ENSP00000234071.4:p.Trp273=
ENST00000234071.7:c.819G=	ENSP00000234071.3:p.Trp273=
ENST00000402125.2:c.143G=
ENST00000409048.1:c.921G=	ENSP00000386679.1:p.Trp307=
NM_000312.3:c.819G= , LRG_599t1:c.819G=	NP_000303.1:p.Trp273=
XM_005263715.3:c.1002G=	XP_005263772.1:p.Trp334=
XM_005263716.3:c.984G=	XP_005263773.1:p.Trp328=
XM_005263717.3:c.882G=	XP_005263774.1:p.Trp294=
XR_923313.1:n.1332-115C=
XM_005263717.4:c.882G=	XP_005263774.1:p.Trp294=
XM_017004505.1:c.1062G=	XP_016859994.1:p.Trp354=
XM_024453002.1:c.1164G=	XP_024308770.1:p.Trp388=
XM_024453003.1:c.1104G=	XP_024308771.1:p.Trp368=
XM_024453004.1:c.1002G=	XP_024308772.1:p.Trp334=
XM_024453005.1:c.984G=	XP_024308773.1:p.Trp328=
XM_024453006.1:c.921G=	XP_024308774.1:p.Trp307=
XR_001739705.1:n.3607-115C=
XR_923313.2:n.4043-115C=
NM_000312.4:c.819G= MANE Select	NP_000303.1:p.Trp273=
NM_001375602.1:c.1002G=	NP_001362531.1:p.Trp334=
NM_001375603.1:c.984G=	NP_001362532.1:p.Trp328=
NM_001375604.1:c.882G=	NP_001362533.1:p.Trp294=
NM_001375605.1:c.921G=	NP_001362534.1:p.Trp307=
NM_001375606.1:c.987G=	NP_001362535.1:p.Trp329=
NM_001375607.1:c.1005G=	NP_001362536.1:p.Trp335=
NM_001375608.1:c.762G=	NP_001362537.1:p.Trp254=
NM_001375609.1:c.795G=	NP_001362538.1:p.Trp265=
NM_001375610.1:c.813G=	NP_001362539.1:p.Trp271=
NM_001375611.1:c.819G=	NP_001362540.1:p.Trp273=
NM_001375613.1:c.819G=	NP_001362542.1:p.Trp273=