Canonical Allele Identifier: CA1286884615
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428736G= , CM000664.2:g.127428736G= GRCh38
NC_000002.11:g.128186312G= , CM000664.1:g.128186312G= GRCh37
NC_000002.10:g.127902782G= NCBI36
NG_016323.1:g.15317G= , LRG_599:g.15317G=

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.1176G= MANE Select ENSP00000234071.4:p.Gly392=
ENST00000234071.7:c.1176G= ENSP00000234071.3:p.Gly392=
ENST00000402125.2:c.500G=
ENST00000409048.1:c.1278G= ENSP00000386679.1:p.Gly426=
NM_000312.3:c.1176G= , LRG_599t1:c.1176G= NP_000303.1:p.Gly392=
XM_005263715.3:c.1359G= XP_005263772.1:p.Gly453=
XM_005263716.3:c.1341G= XP_005263773.1:p.Gly447=
XM_005263717.3:c.1239G= XP_005263774.1:p.Gly413=
XR_923313.1:n.1332-472C=
XM_005263717.4:c.1239G= XP_005263774.1:p.Gly413=
XM_017004505.1:c.1419G= XP_016859994.1:p.Gly473=
XM_024453002.1:c.1521G= XP_024308770.1:p.Gly507=
XM_024453003.1:c.1461G= XP_024308771.1:p.Gly487=
XM_024453004.1:c.1359G= XP_024308772.1:p.Gly453=
XM_024453005.1:c.1341G= XP_024308773.1:p.Gly447=
XM_024453006.1:c.1278G= XP_024308774.1:p.Gly426=
XR_001739705.1:n.3607-472C=
XR_923313.2:n.4043-472C=
NM_000312.4:c.1176G= MANE Select NP_000303.1:p.Gly392=
NM_001375602.1:c.1359G= NP_001362531.1:p.Gly453=
NM_001375603.1:c.1341G= NP_001362532.1:p.Gly447=
NM_001375604.1:c.1239G= NP_001362533.1:p.Gly413=
NM_001375605.1:c.1278G= NP_001362534.1:p.Gly426=
NM_001375606.1:c.1344G= NP_001362535.1:p.Gly448=
NM_001375607.1:c.1362G= NP_001362536.1:p.Gly454=
NM_001375608.1:c.1119G= NP_001362537.1:p.Gly373=
NM_001375609.1:c.1152G= NP_001362538.1:p.Gly384=
NM_001375610.1:c.1170G= NP_001362539.1:p.Gly390=
NM_001375611.1:c.1176G= NP_001362540.1:p.Gly392=
NM_001375613.1:c.1176G= NP_001362542.1:p.Gly392=