Canonical Allele Identifier: CA1286884452
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428409G= , CM000664.2:g.127428409G= GRCh38
NC_000002.11:g.128185985G= , CM000664.1:g.128185985G= GRCh37
NC_000002.10:g.127902455G= NCBI36
NG_016323.1:g.14990G= , LRG_599:g.14990G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.849G= MANE Select ENSP00000234071.4:p.Lys283=
ENST00000234071.7:c.849G= ENSP00000234071.3:p.Lys283=
ENST00000402125.2:c.173G=
ENST00000409048.1:c.951G= ENSP00000386679.1:p.Lys317=
NM_000312.3:c.849G= , LRG_599t1:c.849G= NP_000303.1:p.Lys283=
XM_005263715.3:c.1032G= XP_005263772.1:p.Lys344=
XM_005263716.3:c.1014G= XP_005263773.1:p.Lys338=
XM_005263717.3:c.912G= XP_005263774.1:p.Lys304=
XR_923313.1:n.1332-145C=
XM_005263717.4:c.912G= XP_005263774.1:p.Lys304=
XM_017004505.1:c.1092G= XP_016859994.1:p.Lys364=
XM_024453002.1:c.1194G= XP_024308770.1:p.Lys398=
XM_024453003.1:c.1134G= XP_024308771.1:p.Lys378=
XM_024453004.1:c.1032G= XP_024308772.1:p.Lys344=
XM_024453005.1:c.1014G= XP_024308773.1:p.Lys338=
XM_024453006.1:c.951G= XP_024308774.1:p.Lys317=
XR_001739705.1:n.3607-145C=
XR_923313.2:n.4043-145C=
NM_000312.4:c.849G= MANE Select NP_000303.1:p.Lys283=
NM_001375602.1:c.1032G= NP_001362531.1:p.Lys344=
NM_001375603.1:c.1014G= NP_001362532.1:p.Lys338=
NM_001375604.1:c.912G= NP_001362533.1:p.Lys304=
NM_001375605.1:c.951G= NP_001362534.1:p.Lys317=
NM_001375606.1:c.1017G= NP_001362535.1:p.Lys339=
NM_001375607.1:c.1035G= NP_001362536.1:p.Lys345=
NM_001375608.1:c.792G= NP_001362537.1:p.Lys264=
NM_001375609.1:c.825G= NP_001362538.1:p.Lys275=
NM_001375610.1:c.843G= NP_001362539.1:p.Lys281=
NM_001375611.1:c.849G= NP_001362540.1:p.Lys283=
NM_001375613.1:c.849G= NP_001362542.1:p.Lys283=