Canonical Allele Identifier: CA1286884668

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428824T= , CM000664.2:g.127428824T=	GRCh38
NC_000002.11:g.128186400T= , CM000664.1:g.128186400T=	GRCh37
NC_000002.10:g.127902870T=	NCBI36
NG_016323.1:g.15405T= , LRG_599:g.15405T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1264T= MANE Select	ENSP00000234071.4:p.Trp422=
ENST00000234071.7:c.1264T=	ENSP00000234071.3:p.Trp422=
ENST00000402125.2:c.588T=
ENST00000409048.1:c.1366T=	ENSP00000386679.1:p.Trp456=
NM_000312.3:c.1264T= , LRG_599t1:c.1264T=	NP_000303.1:p.Trp422=
XM_005263715.3:c.1447T=	XP_005263772.1:p.Trp483=
XM_005263716.3:c.1429T=	XP_005263773.1:p.Trp477=
XM_005263717.3:c.1327T=	XP_005263774.1:p.Trp443=
XR_923313.1:n.1332-560A=
XM_005263717.4:c.1327T=	XP_005263774.1:p.Trp443=
XM_017004505.1:c.1507T=	XP_016859994.1:p.Trp503=
XM_024453002.1:c.1609T=	XP_024308770.1:p.Trp537=
XM_024453003.1:c.1549T=	XP_024308771.1:p.Trp517=
XM_024453004.1:c.1447T=	XP_024308772.1:p.Trp483=
XM_024453005.1:c.1429T=	XP_024308773.1:p.Trp477=
XM_024453006.1:c.1366T=	XP_024308774.1:p.Trp456=
XR_001739705.1:n.3607-560A=
XR_923313.2:n.4043-560A=
NM_000312.4:c.1264T= MANE Select	NP_000303.1:p.Trp422=
NM_001375602.1:c.1447T=	NP_001362531.1:p.Trp483=
NM_001375603.1:c.1429T=	NP_001362532.1:p.Trp477=
NM_001375604.1:c.1327T=	NP_001362533.1:p.Trp443=
NM_001375605.1:c.1366T=	NP_001362534.1:p.Trp456=
NM_001375606.1:c.1432T=	NP_001362535.1:p.Trp478=
NM_001375607.1:c.1450T=	NP_001362536.1:p.Trp484=
NM_001375608.1:c.1207T=	NP_001362537.1:p.Trp403=
NM_001375609.1:c.1240T=	NP_001362538.1:p.Trp414=
NM_001375610.1:c.1258T=	NP_001362539.1:p.Trp420=
NM_001375611.1:c.1264T=	NP_001362540.1:p.Trp422=
NM_001375613.1:c.1264T=	NP_001362542.1:p.Trp422=