Canonical Allele Identifier: CA1286883455
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426218C= , CM000664.2:g.127426218C= GRCh38
NC_000002.11:g.128183794C= , CM000664.1:g.128183794C= GRCh37
NC_000002.10:g.127900264C= NCBI36
NG_016323.1:g.12799C= , LRG_599:g.12799C=

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.669C= MANE Select ENSP00000234071.4:p.Ser223=
ENST00000234071.7:c.669C= ENSP00000234071.3:p.Ser223=
ENST00000402125.2:c.121-2139C=
ENST00000409048.1:c.771C= ENSP00000386679.1:p.Ser257=
ENST00000464089.1:n.255C=
NM_000312.3:c.669C= , LRG_599t1:c.669C= NP_000303.1:p.Ser223=
XM_005263715.3:c.852C= XP_005263772.1:p.Ser284=
XM_005263716.3:c.834C= XP_005263773.1:p.Ser278=
XM_005263717.3:c.732C= XP_005263774.1:p.Ser244=
XM_005263717.4:c.732C= XP_005263774.1:p.Ser244=
XM_017004505.1:c.912C= XP_016859994.1:p.Ser304=
XM_024453002.1:c.1014C= XP_024308770.1:p.Ser338=
XM_024453003.1:c.954C= XP_024308771.1:p.Ser318=
XM_024453004.1:c.852C= XP_024308772.1:p.Ser284=
XM_024453005.1:c.834C= XP_024308773.1:p.Ser278=
XM_024453006.1:c.771C= XP_024308774.1:p.Ser257=
XR_923313.2:n.4367G=
NM_000312.4:c.669C= MANE Select NP_000303.1:p.Ser223=
NM_001375602.1:c.852C= NP_001362531.1:p.Ser284=
NM_001375603.1:c.834C= NP_001362532.1:p.Ser278=
NM_001375604.1:c.732C= NP_001362533.1:p.Ser244=
NM_001375605.1:c.771C= NP_001362534.1:p.Ser257=
NM_001375606.1:c.837C= NP_001362535.1:p.Ser279=
NM_001375607.1:c.855C= NP_001362536.1:p.Ser285=
NM_001375608.1:c.612C= NP_001362537.1:p.Ser204=
NM_001375609.1:c.645C= NP_001362538.1:p.Ser215=
NM_001375610.1:c.663C= NP_001362539.1:p.Ser221=
NM_001375611.1:c.669C= NP_001362540.1:p.Ser223=
NM_001375613.1:c.669C= NP_001362542.1:p.Ser223=