Canonical Allele Identifier: CA348399243
Gene: PROC HGNC NCBI

Linked Data

dbSNP Id: rs2104953477

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127423186T>G , CM000664.2:g.127423186T>G GRCh38
NC_000002.11:g.128180762T>G , CM000664.1:g.128180762T>G GRCh37
NC_000002.10:g.127897232T>G NCBI36
NG_016323.1:g.9767T>G , LRG_599:g.9767T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.400+15T>G MANE Select ENSP00000234071.4:n.400+15T>G
ENST00000234071.7:c.400+15T>G ENSP00000234071.3:n.400+15T>G
ENST00000409048.1:c.415T>G ENSP00000386679.1:p.Trp139Gly
ENST00000419985.5:c.*221T>G ENSP00000392606.1:n.*221T>G
ENST00000442644.5:c.400+15T>G ENSP00000411241.1:n.400+15T>G
NM_000312.3:c.400+15T>G , LRG_599t1:c.400+15T>G NP_000303.1:n.400+15T>G
XM_005263715.3:c.583+15T>G XP_005263772.1:n.583+15T>G
XM_005263716.3:c.478T>G XP_005263773.1:p.Trp160Gly
XM_005263717.3:c.463+15T>G XP_005263774.1:n.463+15T>G
XM_005263717.4:c.463+15T>G XP_005263774.1:n.463+15T>G
XM_017004505.1:c.643+15T>G XP_016859994.1:n.643+15T>G
XM_024453002.1:c.658T>G XP_024308770.1:p.Trp220Gly
XM_024453003.1:c.598T>G XP_024308771.1:p.Trp200Gly
XM_024453004.1:c.583+15T>G XP_024308772.1:n.583+15T>G
XM_024453005.1:c.478T>G XP_024308773.1:p.Trp160Gly
XM_024453006.1:c.415T>G XP_024308774.1:p.Trp139Gly
NM_000312.4:c.400+15T>G MANE Select NP_000303.1:n.400+15T>G
NM_001375602.1:c.583+15T>G NP_001362531.1:n.583+15T>G
NM_001375603.1:c.478T>G NP_001362532.1:p.Trp160Gly
NM_001375604.1:c.463+15T>G NP_001362533.1:n.463+15T>G
NM_001375605.1:c.415T>G NP_001362534.1:p.Trp139Gly
NM_001375606.1:c.568+2T>G NP_001362535.1:n.568+2T>G
NM_001375607.1:c.499T>G NP_001362536.1:p.Trp167Gly
NM_001375608.1:c.400+15T>G NP_001362537.1:n.400+15T>G
NM_001375609.1:c.376+15T>G NP_001362538.1:n.376+15T>G
NM_001375610.1:c.394+15T>G NP_001362539.1:n.394+15T>G
NM_001375611.1:c.400+15T>G NP_001362540.1:n.400+15T>G
NM_001375613.1:c.400+15T>G NP_001362542.1:n.400+15T>G