Canonical Allele Identifier: CA1859568
Gene: PROC HGNC NCBI

Linked Data

ClinVar Variation Id: 706791
dbSNP Id: rs748650244

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428886C>T , CM000664.2:g.127428886C>T GRCh38
NC_000002.11:g.128186462C>T , CM000664.1:g.128186462C>T GRCh37
NC_000002.10:g.127902932C>T NCBI36
NG_016323.1:g.15467C>T , LRG_599:g.15467C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.1326C>T MANE Select ENSP00000234071.4:p.Leu442=
ENST00000234071.7:c.1326C>T ENSP00000234071.3:p.Leu442=
ENST00000402125.2:c.650C>T
ENST00000409048.1:c.1428C>T ENSP00000386679.1:p.Leu476=
NM_000312.3:c.1326C>T , LRG_599t1:c.1326C>T NP_000303.1:p.Leu442=
XM_005263715.3:c.1509C>T XP_005263772.1:p.Leu503=
XM_005263716.3:c.1491C>T XP_005263773.1:p.Leu497=
XM_005263717.3:c.1389C>T XP_005263774.1:p.Leu463=
XR_923313.1:n.1332-622G>A
XM_005263717.4:c.1389C>T XP_005263774.1:p.Leu463=
XM_017004505.1:c.1569C>T XP_016859994.1:p.Leu523=
XM_024453002.1:c.1671C>T XP_024308770.1:p.Leu557=
XM_024453003.1:c.1611C>T XP_024308771.1:p.Leu537=
XM_024453004.1:c.1509C>T XP_024308772.1:p.Leu503=
XM_024453005.1:c.1491C>T XP_024308773.1:p.Leu497=
XM_024453006.1:c.1428C>T XP_024308774.1:p.Leu476=
XR_001739705.1:n.3607-622G>A
XR_923313.2:n.4043-622G>A
NM_000312.4:c.1326C>T MANE Select NP_000303.1:p.Leu442=
NM_001375602.1:c.1509C>T NP_001362531.1:p.Leu503=
NM_001375603.1:c.1491C>T NP_001362532.1:p.Leu497=
NM_001375604.1:c.1389C>T NP_001362533.1:p.Leu463=
NM_001375605.1:c.1428C>T NP_001362534.1:p.Leu476=
NM_001375606.1:c.1494C>T NP_001362535.1:p.Leu498=
NM_001375607.1:c.1512C>T NP_001362536.1:p.Leu504=
NM_001375608.1:c.1269C>T NP_001362537.1:p.Leu423=
NM_001375609.1:c.1302C>T NP_001362538.1:p.Leu434=
NM_001375610.1:c.1320C>T NP_001362539.1:p.Leu440=
NM_001375611.1:c.1326C>T NP_001362540.1:p.Leu442=
NM_001375613.1:c.1326C>T NP_001362542.1:p.Leu442=