Canonical Allele Identifier: CA348405784
Gene: PROC HGNC NCBI

Linked Data

dbSNP Id: rs1355168080

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428657C>T , CM000664.2:g.127428657C>T GRCh38
NC_000002.11:g.128186233C>T , CM000664.1:g.128186233C>T GRCh37
NC_000002.10:g.127902703C>T NCBI36
NG_016323.1:g.15238C>T , LRG_599:g.15238C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.1097C>T MANE Select ENSP00000234071.4:p.Pro366Leu
ENST00000234071.7:c.1097C>T ENSP00000234071.3:p.Pro366Leu
ENST00000402125.2:c.421C>T
ENST00000409048.1:c.1199C>T ENSP00000386679.1:p.Pro400Leu
NM_000312.3:c.1097C>T , LRG_599t1:c.1097C>T NP_000303.1:p.Pro366Leu
XM_005263715.3:c.1280C>T XP_005263772.1:p.Pro427Leu
XM_005263716.3:c.1262C>T XP_005263773.1:p.Pro421Leu
XM_005263717.3:c.1160C>T XP_005263774.1:p.Pro387Leu
XR_923313.1:n.1332-393G>A
XM_005263717.4:c.1160C>T XP_005263774.1:p.Pro387Leu
XM_017004505.1:c.1340C>T XP_016859994.1:p.Pro447Leu
XM_024453002.1:c.1442C>T XP_024308770.1:p.Pro481Leu
XM_024453003.1:c.1382C>T XP_024308771.1:p.Pro461Leu
XM_024453004.1:c.1280C>T XP_024308772.1:p.Pro427Leu
XM_024453005.1:c.1262C>T XP_024308773.1:p.Pro421Leu
XM_024453006.1:c.1199C>T XP_024308774.1:p.Pro400Leu
XR_001739705.1:n.3607-393G>A
XR_923313.2:n.4043-393G>A
NM_000312.4:c.1097C>T MANE Select NP_000303.1:p.Pro366Leu
NM_001375602.1:c.1280C>T NP_001362531.1:p.Pro427Leu
NM_001375603.1:c.1262C>T NP_001362532.1:p.Pro421Leu
NM_001375604.1:c.1160C>T NP_001362533.1:p.Pro387Leu
NM_001375605.1:c.1199C>T NP_001362534.1:p.Pro400Leu
NM_001375606.1:c.1265C>T NP_001362535.1:p.Pro422Leu
NM_001375607.1:c.1283C>T NP_001362536.1:p.Pro428Leu
NM_001375608.1:c.1040C>T NP_001362537.1:p.Pro347Leu
NM_001375609.1:c.1073C>T NP_001362538.1:p.Pro358Leu
NM_001375610.1:c.1091C>T NP_001362539.1:p.Pro364Leu
NM_001375611.1:c.1097C>T NP_001362540.1:p.Pro366Leu
NM_001375613.1:c.1097C>T NP_001362542.1:p.Pro366Leu