Canonical Allele Identifier: CA1859560
Gene: PROC HGNC NCBI

Linked Data

dbSNP Id: rs761888935

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428848C>T , CM000664.2:g.127428848C>T GRCh38
NC_000002.11:g.128186424C>T , CM000664.1:g.128186424C>T GRCh37
NC_000002.10:g.127902894C>T NCBI36
NG_016323.1:g.15429C>T , LRG_599:g.15429C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.1288C>T MANE Select ENSP00000234071.4:p.His430Tyr
ENST00000234071.7:c.1288C>T ENSP00000234071.3:p.His430Tyr
ENST00000402125.2:c.612C>T
ENST00000409048.1:c.1390C>T ENSP00000386679.1:p.His464Tyr
NM_000312.3:c.1288C>T , LRG_599t1:c.1288C>T NP_000303.1:p.His430Tyr
XM_005263715.3:c.1471C>T XP_005263772.1:p.His491Tyr
XM_005263716.3:c.1453C>T XP_005263773.1:p.His485Tyr
XM_005263717.3:c.1351C>T XP_005263774.1:p.His451Tyr
XR_923313.1:n.1332-584G>A
XM_005263717.4:c.1351C>T XP_005263774.1:p.His451Tyr
XM_017004505.1:c.1531C>T XP_016859994.1:p.His511Tyr
XM_024453002.1:c.1633C>T XP_024308770.1:p.His545Tyr
XM_024453003.1:c.1573C>T XP_024308771.1:p.His525Tyr
XM_024453004.1:c.1471C>T XP_024308772.1:p.His491Tyr
XM_024453005.1:c.1453C>T XP_024308773.1:p.His485Tyr
XM_024453006.1:c.1390C>T XP_024308774.1:p.His464Tyr
XR_001739705.1:n.3607-584G>A
XR_923313.2:n.4043-584G>A
NM_000312.4:c.1288C>T MANE Select NP_000303.1:p.His430Tyr
NM_001375602.1:c.1471C>T NP_001362531.1:p.His491Tyr
NM_001375603.1:c.1453C>T NP_001362532.1:p.His485Tyr
NM_001375604.1:c.1351C>T NP_001362533.1:p.His451Tyr
NM_001375605.1:c.1390C>T NP_001362534.1:p.His464Tyr
NM_001375606.1:c.1456C>T NP_001362535.1:p.His486Tyr
NM_001375607.1:c.1474C>T NP_001362536.1:p.His492Tyr
NM_001375608.1:c.1231C>T NP_001362537.1:p.His411Tyr
NM_001375609.1:c.1264C>T NP_001362538.1:p.His422Tyr
NM_001375610.1:c.1282C>T NP_001362539.1:p.His428Tyr
NM_001375611.1:c.1288C>T NP_001362540.1:p.His430Tyr
NM_001375613.1:c.1288C>T NP_001362542.1:p.His430Tyr