Canonical Allele Identifier: CA1286884616
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428737G= , CM000664.2:g.127428737G= GRCh38
NC_000002.11:g.128186313G= , CM000664.1:g.128186313G= GRCh37
NC_000002.10:g.127902783G= NCBI36
NG_016323.1:g.15318G= , LRG_599:g.15318G=

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.1177G= MANE Select ENSP00000234071.4:p.Asp393=
ENST00000234071.7:c.1177G= ENSP00000234071.3:p.Asp393=
ENST00000402125.2:c.501G=
ENST00000409048.1:c.1279G= ENSP00000386679.1:p.Asp427=
NM_000312.3:c.1177G= , LRG_599t1:c.1177G= NP_000303.1:p.Asp393=
XM_005263715.3:c.1360G= XP_005263772.1:p.Asp454=
XM_005263716.3:c.1342G= XP_005263773.1:p.Asp448=
XM_005263717.3:c.1240G= XP_005263774.1:p.Asp414=
XR_923313.1:n.1332-473C=
XM_005263717.4:c.1240G= XP_005263774.1:p.Asp414=
XM_017004505.1:c.1420G= XP_016859994.1:p.Asp474=
XM_024453002.1:c.1522G= XP_024308770.1:p.Asp508=
XM_024453003.1:c.1462G= XP_024308771.1:p.Asp488=
XM_024453004.1:c.1360G= XP_024308772.1:p.Asp454=
XM_024453005.1:c.1342G= XP_024308773.1:p.Asp448=
XM_024453006.1:c.1279G= XP_024308774.1:p.Asp427=
XR_001739705.1:n.3607-473C=
XR_923313.2:n.4043-473C=
NM_000312.4:c.1177G= MANE Select NP_000303.1:p.Asp393=
NM_001375602.1:c.1360G= NP_001362531.1:p.Asp454=
NM_001375603.1:c.1342G= NP_001362532.1:p.Asp448=
NM_001375604.1:c.1240G= NP_001362533.1:p.Asp414=
NM_001375605.1:c.1279G= NP_001362534.1:p.Asp427=
NM_001375606.1:c.1345G= NP_001362535.1:p.Asp449=
NM_001375607.1:c.1363G= NP_001362536.1:p.Asp455=
NM_001375608.1:c.1120G= NP_001362537.1:p.Asp374=
NM_001375609.1:c.1153G= NP_001362538.1:p.Asp385=
NM_001375610.1:c.1171G= NP_001362539.1:p.Asp391=
NM_001375611.1:c.1177G= NP_001362540.1:p.Asp393=
NM_001375613.1:c.1177G= NP_001362542.1:p.Asp393=