Canonical Allele Identifier: CA1859547
Gene: PROC HGNC NCBI

Linked Data

dbSNP Id: rs758788677

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428777T>A , CM000664.2:g.127428777T>A GRCh38
NC_000002.11:g.128186353T>A , CM000664.1:g.128186353T>A GRCh37
NC_000002.10:g.127902823T>A NCBI36
NG_016323.1:g.15358T>A , LRG_599:g.15358T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.1217T>A MANE Select ENSP00000234071.4:p.Met406Lys
ENST00000234071.7:c.1217T>A ENSP00000234071.3:p.Met406Lys
ENST00000402125.2:c.541T>A
ENST00000409048.1:c.1319T>A ENSP00000386679.1:p.Met440Lys
NM_000312.3:c.1217T>A , LRG_599t1:c.1217T>A NP_000303.1:p.Met406Lys
XM_005263715.3:c.1400T>A XP_005263772.1:p.Met467Lys
XM_005263716.3:c.1382T>A XP_005263773.1:p.Met461Lys
XM_005263717.3:c.1280T>A XP_005263774.1:p.Met427Lys
XR_923313.1:n.1332-513A>T
XM_005263717.4:c.1280T>A XP_005263774.1:p.Met427Lys
XM_017004505.1:c.1460T>A XP_016859994.1:p.Met487Lys
XM_024453002.1:c.1562T>A XP_024308770.1:p.Met521Lys
XM_024453003.1:c.1502T>A XP_024308771.1:p.Met501Lys
XM_024453004.1:c.1400T>A XP_024308772.1:p.Met467Lys
XM_024453005.1:c.1382T>A XP_024308773.1:p.Met461Lys
XM_024453006.1:c.1319T>A XP_024308774.1:p.Met440Lys
XR_001739705.1:n.3607-513A>T
XR_923313.2:n.4043-513A>T
NM_000312.4:c.1217T>A MANE Select NP_000303.1:p.Met406Lys
NM_001375602.1:c.1400T>A NP_001362531.1:p.Met467Lys
NM_001375603.1:c.1382T>A NP_001362532.1:p.Met461Lys
NM_001375604.1:c.1280T>A NP_001362533.1:p.Met427Lys
NM_001375605.1:c.1319T>A NP_001362534.1:p.Met440Lys
NM_001375606.1:c.1385T>A NP_001362535.1:p.Met462Lys
NM_001375607.1:c.1403T>A NP_001362536.1:p.Met468Lys
NM_001375608.1:c.1160T>A NP_001362537.1:p.Met387Lys
NM_001375609.1:c.1193T>A NP_001362538.1:p.Met398Lys
NM_001375610.1:c.1211T>A NP_001362539.1:p.Met404Lys
NM_001375611.1:c.1217T>A NP_001362540.1:p.Met406Lys
NM_001375613.1:c.1217T>A NP_001362542.1:p.Met406Lys