Canonical Allele Identifier: CA1286884585

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428680A= , CM000664.2:g.127428680A=	GRCh38
NC_000002.11:g.128186256A= , CM000664.1:g.128186256A=	GRCh37
NC_000002.10:g.127902726A=	NCBI36
NG_016323.1:g.15261A= , LRG_599:g.15261A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1120A= MANE Select	ENSP00000234071.4:p.Ser374=
ENST00000234071.7:c.1120A=	ENSP00000234071.3:p.Ser374=
ENST00000402125.2:c.444A=
ENST00000409048.1:c.1222A=	ENSP00000386679.1:p.Ser408=
NM_000312.3:c.1120A= , LRG_599t1:c.1120A=	NP_000303.1:p.Ser374=
XM_005263715.3:c.1303A=	XP_005263772.1:p.Ser435=
XM_005263716.3:c.1285A=	XP_005263773.1:p.Ser429=
XM_005263717.3:c.1183A=	XP_005263774.1:p.Ser395=
XR_923313.1:n.1332-416T=
XM_005263717.4:c.1183A=	XP_005263774.1:p.Ser395=
XM_017004505.1:c.1363A=	XP_016859994.1:p.Ser455=
XM_024453002.1:c.1465A=	XP_024308770.1:p.Ser489=
XM_024453003.1:c.1405A=	XP_024308771.1:p.Ser469=
XM_024453004.1:c.1303A=	XP_024308772.1:p.Ser435=
XM_024453005.1:c.1285A=	XP_024308773.1:p.Ser429=
XM_024453006.1:c.1222A=	XP_024308774.1:p.Ser408=
XR_001739705.1:n.3607-416T=
XR_923313.2:n.4043-416T=
NM_000312.4:c.1120A= MANE Select	NP_000303.1:p.Ser374=
NM_001375602.1:c.1303A=	NP_001362531.1:p.Ser435=
NM_001375603.1:c.1285A=	NP_001362532.1:p.Ser429=
NM_001375604.1:c.1183A=	NP_001362533.1:p.Ser395=
NM_001375605.1:c.1222A=	NP_001362534.1:p.Ser408=
NM_001375606.1:c.1288A=	NP_001362535.1:p.Ser430=
NM_001375607.1:c.1306A=	NP_001362536.1:p.Ser436=
NM_001375608.1:c.1063A=	NP_001362537.1:p.Ser355=
NM_001375609.1:c.1096A=	NP_001362538.1:p.Ser366=
NM_001375610.1:c.1114A=	NP_001362539.1:p.Ser372=
NM_001375611.1:c.1120A=	NP_001362540.1:p.Ser374=
NM_001375613.1:c.1120A=	NP_001362542.1:p.Ser374=