Canonical Allele Identifier: CA1286884549
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428609A= , CM000664.2:g.127428609A= GRCh38
NC_000002.11:g.128186185A= , CM000664.1:g.128186185A= GRCh37
NC_000002.10:g.127902655A= NCBI36
NG_016323.1:g.15190A= , LRG_599:g.15190A=

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.1049A= MANE Select ENSP00000234071.4:p.Lys350=
ENST00000234071.7:c.1049A= ENSP00000234071.3:p.Lys350=
ENST00000402125.2:c.373A=
ENST00000409048.1:c.1151A= ENSP00000386679.1:p.Lys384=
NM_000312.3:c.1049A= , LRG_599t1:c.1049A= NP_000303.1:p.Lys350=
XM_005263715.3:c.1232A= XP_005263772.1:p.Lys411=
XM_005263716.3:c.1214A= XP_005263773.1:p.Lys405=
XM_005263717.3:c.1112A= XP_005263774.1:p.Lys371=
XR_923313.1:n.1332-345T=
XM_005263717.4:c.1112A= XP_005263774.1:p.Lys371=
XM_017004505.1:c.1292A= XP_016859994.1:p.Lys431=
XM_024453002.1:c.1394A= XP_024308770.1:p.Lys465=
XM_024453003.1:c.1334A= XP_024308771.1:p.Lys445=
XM_024453004.1:c.1232A= XP_024308772.1:p.Lys411=
XM_024453005.1:c.1214A= XP_024308773.1:p.Lys405=
XM_024453006.1:c.1151A= XP_024308774.1:p.Lys384=
XR_001739705.1:n.3607-345T=
XR_923313.2:n.4043-345T=
NM_000312.4:c.1049A= MANE Select NP_000303.1:p.Lys350=
NM_001375602.1:c.1232A= NP_001362531.1:p.Lys411=
NM_001375603.1:c.1214A= NP_001362532.1:p.Lys405=
NM_001375604.1:c.1112A= NP_001362533.1:p.Lys371=
NM_001375605.1:c.1151A= NP_001362534.1:p.Lys384=
NM_001375606.1:c.1217A= NP_001362535.1:p.Lys406=
NM_001375607.1:c.1235A= NP_001362536.1:p.Lys412=
NM_001375608.1:c.992A= NP_001362537.1:p.Lys331=
NM_001375609.1:c.1025A= NP_001362538.1:p.Lys342=
NM_001375610.1:c.1043A= NP_001362539.1:p.Lys348=
NM_001375611.1:c.1049A= NP_001362540.1:p.Lys350=
NM_001375613.1:c.1049A= NP_001362542.1:p.Lys350=