Canonical Allele Identifier: CA1286883413
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426122G= , CM000664.2:g.127426122G= GRCh38
NC_000002.11:g.128183698G= , CM000664.1:g.128183698G= GRCh37
NC_000002.10:g.127900168G= NCBI36
NG_016323.1:g.12703G= , LRG_599:g.12703G=

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.573G= MANE Select ENSP00000234071.4:p.Glu191=
ENST00000234071.7:c.573G= ENSP00000234071.3:p.Glu191=
ENST00000402125.2:c.121-2235G=
ENST00000409048.1:c.675G= ENSP00000386679.1:p.Glu225=
ENST00000442644.5:c.516G= ENSP00000411241.1:p.Glu172=
ENST00000464089.1:n.159G=
NM_000312.3:c.573G= , LRG_599t1:c.573G= NP_000303.1:p.Glu191=
XM_005263715.3:c.756G= XP_005263772.1:p.Glu252=
XM_005263716.3:c.738G= XP_005263773.1:p.Glu246=
XM_005263717.3:c.636G= XP_005263774.1:p.Glu212=
XM_005263717.4:c.636G= XP_005263774.1:p.Glu212=
XM_017004505.1:c.816G= XP_016859994.1:p.Glu272=
XM_024453002.1:c.918G= XP_024308770.1:p.Glu306=
XM_024453003.1:c.858G= XP_024308771.1:p.Glu286=
XM_024453004.1:c.756G= XP_024308772.1:p.Glu252=
XM_024453005.1:c.738G= XP_024308773.1:p.Glu246=
XM_024453006.1:c.675G= XP_024308774.1:p.Glu225=
XR_923313.2:n.4463C=
NM_000312.4:c.573G= MANE Select NP_000303.1:p.Glu191=
NM_001375602.1:c.756G= NP_001362531.1:p.Glu252=
NM_001375603.1:c.738G= NP_001362532.1:p.Glu246=
NM_001375604.1:c.636G= NP_001362533.1:p.Glu212=
NM_001375605.1:c.675G= NP_001362534.1:p.Glu225=
NM_001375606.1:c.741G= NP_001362535.1:p.Glu247=
NM_001375607.1:c.759G= NP_001362536.1:p.Glu253=
NM_001375608.1:c.516G= NP_001362537.1:p.Glu172=
NM_001375609.1:c.549G= NP_001362538.1:p.Glu183=
NM_001375610.1:c.567G= NP_001362539.1:p.Glu189=
NM_001375611.1:c.573G= NP_001362540.1:p.Glu191=
NM_001375613.1:c.573G= NP_001362542.1:p.Glu191=