Canonical Allele Identifier: CA1286884489
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428471A= , CM000664.2:g.127428471A= GRCh38
NC_000002.11:g.128186047A= , CM000664.1:g.128186047A= GRCh37
NC_000002.10:g.127902517A= NCBI36
NG_016323.1:g.15052A= , LRG_599:g.15052A=

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.911A= MANE Select ENSP00000234071.4:p.His304=
ENST00000234071.7:c.911A= ENSP00000234071.3:p.His304=
ENST00000402125.2:c.235A=
ENST00000409048.1:c.1013A= ENSP00000386679.1:p.His338=
NM_000312.3:c.911A= , LRG_599t1:c.911A= NP_000303.1:p.His304=
XM_005263715.3:c.1094A= XP_005263772.1:p.His365=
XM_005263716.3:c.1076A= XP_005263773.1:p.His359=
XM_005263717.3:c.974A= XP_005263774.1:p.His325=
XR_923313.1:n.1332-207T=
XM_005263717.4:c.974A= XP_005263774.1:p.His325=
XM_017004505.1:c.1154A= XP_016859994.1:p.His385=
XM_024453002.1:c.1256A= XP_024308770.1:p.His419=
XM_024453003.1:c.1196A= XP_024308771.1:p.His399=
XM_024453004.1:c.1094A= XP_024308772.1:p.His365=
XM_024453005.1:c.1076A= XP_024308773.1:p.His359=
XM_024453006.1:c.1013A= XP_024308774.1:p.His338=
XR_001739705.1:n.3607-207T=
XR_923313.2:n.4043-207T=
NM_000312.4:c.911A= MANE Select NP_000303.1:p.His304=
NM_001375602.1:c.1094A= NP_001362531.1:p.His365=
NM_001375603.1:c.1076A= NP_001362532.1:p.His359=
NM_001375604.1:c.974A= NP_001362533.1:p.His325=
NM_001375605.1:c.1013A= NP_001362534.1:p.His338=
NM_001375606.1:c.1079A= NP_001362535.1:p.His360=
NM_001375607.1:c.1097A= NP_001362536.1:p.His366=
NM_001375608.1:c.854A= NP_001362537.1:p.His285=
NM_001375609.1:c.887A= NP_001362538.1:p.His296=
NM_001375610.1:c.905A= NP_001362539.1:p.His302=
NM_001375611.1:c.911A= NP_001362540.1:p.His304=
NM_001375613.1:c.911A= NP_001362542.1:p.His304=