Canonical Allele Identifier: CA1286883406
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426112A= , CM000664.2:g.127426112A= GRCh38
NC_000002.11:g.128183688A= , CM000664.1:g.128183688A= GRCh37
NC_000002.10:g.127900158A= NCBI36
NG_016323.1:g.12693A= , LRG_599:g.12693A=

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.563A= MANE Select ENSP00000234071.4:p.Lys188=
ENST00000234071.7:c.563A= ENSP00000234071.3:p.Lys188=
ENST00000402125.2:c.121-2245A=
ENST00000409048.1:c.665A= ENSP00000386679.1:p.Lys222=
ENST00000442644.5:c.506A= ENSP00000411241.1:p.Lys169=
ENST00000464089.1:n.149A=
NM_000312.3:c.563A= , LRG_599t1:c.563A= NP_000303.1:p.Lys188=
XM_005263715.3:c.746A= XP_005263772.1:p.Lys249=
XM_005263716.3:c.728A= XP_005263773.1:p.Lys243=
XM_005263717.3:c.626A= XP_005263774.1:p.Lys209=
XM_005263717.4:c.626A= XP_005263774.1:p.Lys209=
XM_017004505.1:c.806A= XP_016859994.1:p.Lys269=
XM_024453002.1:c.908A= XP_024308770.1:p.Lys303=
XM_024453003.1:c.848A= XP_024308771.1:p.Lys283=
XM_024453004.1:c.746A= XP_024308772.1:p.Lys249=
XM_024453005.1:c.728A= XP_024308773.1:p.Lys243=
XM_024453006.1:c.665A= XP_024308774.1:p.Lys222=
XR_923313.2:n.4473T=
NM_000312.4:c.563A= MANE Select NP_000303.1:p.Lys188=
NM_001375602.1:c.746A= NP_001362531.1:p.Lys249=
NM_001375603.1:c.728A= NP_001362532.1:p.Lys243=
NM_001375604.1:c.626A= NP_001362533.1:p.Lys209=
NM_001375605.1:c.665A= NP_001362534.1:p.Lys222=
NM_001375606.1:c.731A= NP_001362535.1:p.Lys244=
NM_001375607.1:c.749A= NP_001362536.1:p.Lys250=
NM_001375608.1:c.506A= NP_001362537.1:p.Lys169=
NM_001375609.1:c.539A= NP_001362538.1:p.Lys180=
NM_001375610.1:c.557A= NP_001362539.1:p.Lys186=
NM_001375611.1:c.563A= NP_001362540.1:p.Lys188=
NM_001375613.1:c.563A= NP_001362542.1:p.Lys188=