Canonical Allele Identifier: CA1286883423
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426141A= , CM000664.2:g.127426141A= GRCh38
NC_000002.11:g.128183717A= , CM000664.1:g.128183717A= GRCh37
NC_000002.10:g.127900187A= NCBI36
NG_016323.1:g.12722A= , LRG_599:g.12722A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.592A= MANE Select ENSP00000234071.4:p.Lys198=
ENST00000234071.7:c.592A= ENSP00000234071.3:p.Lys198=
ENST00000402125.2:c.121-2216A=
ENST00000409048.1:c.694A= ENSP00000386679.1:p.Lys232=
ENST00000464089.1:n.178A=
NM_000312.3:c.592A= , LRG_599t1:c.592A= NP_000303.1:p.Lys198=
XM_005263715.3:c.775A= XP_005263772.1:p.Lys259=
XM_005263716.3:c.757A= XP_005263773.1:p.Lys253=
XM_005263717.3:c.655A= XP_005263774.1:p.Lys219=
XM_005263717.4:c.655A= XP_005263774.1:p.Lys219=
XM_017004505.1:c.835A= XP_016859994.1:p.Lys279=
XM_024453002.1:c.937A= XP_024308770.1:p.Lys313=
XM_024453003.1:c.877A= XP_024308771.1:p.Lys293=
XM_024453004.1:c.775A= XP_024308772.1:p.Lys259=
XM_024453005.1:c.757A= XP_024308773.1:p.Lys253=
XM_024453006.1:c.694A= XP_024308774.1:p.Lys232=
XR_923313.2:n.4444T=
NM_000312.4:c.592A= MANE Select NP_000303.1:p.Lys198=
NM_001375602.1:c.775A= NP_001362531.1:p.Lys259=
NM_001375603.1:c.757A= NP_001362532.1:p.Lys253=
NM_001375604.1:c.655A= NP_001362533.1:p.Lys219=
NM_001375605.1:c.694A= NP_001362534.1:p.Lys232=
NM_001375606.1:c.760A= NP_001362535.1:p.Lys254=
NM_001375607.1:c.778A= NP_001362536.1:p.Lys260=
NM_001375608.1:c.535A= NP_001362537.1:p.Lys179=
NM_001375609.1:c.568A= NP_001362538.1:p.Lys190=
NM_001375610.1:c.586A= NP_001362539.1:p.Lys196=
NM_001375611.1:c.592A= NP_001362540.1:p.Lys198=
NM_001375613.1:c.592A= NP_001362542.1:p.Lys198=