Canonical Allele Identifier: CA1286884559
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428627G= , CM000664.2:g.127428627G= GRCh38
NC_000002.11:g.128186203G= , CM000664.1:g.128186203G= GRCh37
NC_000002.10:g.127902673G= NCBI36
NG_016323.1:g.15208G= , LRG_599:g.15208G=

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.1067G= MANE Select ENSP00000234071.4:p.Arg356=
ENST00000234071.7:c.1067G= ENSP00000234071.3:p.Arg356=
ENST00000402125.2:c.391G=
ENST00000409048.1:c.1169G= ENSP00000386679.1:p.Arg390=
NM_000312.3:c.1067G= , LRG_599t1:c.1067G= NP_000303.1:p.Arg356=
XM_005263715.3:c.1250G= XP_005263772.1:p.Arg417=
XM_005263716.3:c.1232G= XP_005263773.1:p.Arg411=
XM_005263717.3:c.1130G= XP_005263774.1:p.Arg377=
XR_923313.1:n.1332-363C=
XM_005263717.4:c.1130G= XP_005263774.1:p.Arg377=
XM_017004505.1:c.1310G= XP_016859994.1:p.Arg437=
XM_024453002.1:c.1412G= XP_024308770.1:p.Arg471=
XM_024453003.1:c.1352G= XP_024308771.1:p.Arg451=
XM_024453004.1:c.1250G= XP_024308772.1:p.Arg417=
XM_024453005.1:c.1232G= XP_024308773.1:p.Arg411=
XM_024453006.1:c.1169G= XP_024308774.1:p.Arg390=
XR_001739705.1:n.3607-363C=
XR_923313.2:n.4043-363C=
NM_000312.4:c.1067G= MANE Select NP_000303.1:p.Arg356=
NM_001375602.1:c.1250G= NP_001362531.1:p.Arg417=
NM_001375603.1:c.1232G= NP_001362532.1:p.Arg411=
NM_001375604.1:c.1130G= NP_001362533.1:p.Arg377=
NM_001375605.1:c.1169G= NP_001362534.1:p.Arg390=
NM_001375606.1:c.1235G= NP_001362535.1:p.Arg412=
NM_001375607.1:c.1253G= NP_001362536.1:p.Arg418=
NM_001375608.1:c.1010G= NP_001362537.1:p.Arg337=
NM_001375609.1:c.1043G= NP_001362538.1:p.Arg348=
NM_001375610.1:c.1061G= NP_001362539.1:p.Arg354=
NM_001375611.1:c.1067G= NP_001362540.1:p.Arg356=
NM_001375613.1:c.1067G= NP_001362542.1:p.Arg356=