Canonical Allele Identifier: CA1592022
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 2019425
ClinVar RCV Id: RCV002847094
dbSNP Id: rs373615342
gnomAD v2: 2-29294027-A-G
gnomAD v3: 2-29071161-A-G
gnomAD v4: 2-29071161-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071161A>G , CM000664.2:g.29071161A>G GRCh38
NC_000002.11:g.29294027A>G , CM000664.1:g.29294027A>G GRCh37
NC_000002.10:g.29147531A>G NCBI36
NG_021427.1:g.8101T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3101T>C MANE Select ENSP00000332809.4:p.Val1034Ala
ENST00000331664.5:c.3101T>C ENSP00000332809.4:p.Val1034Ala
NM_001029883.2:c.3101T>C NP_001025054.1:p.Val1034Ala
XM_011532826.1:c.3101T>C XP_011531128.1:p.Val1034Ala
XR_939901.1:n.185+1994A>G
XR_939902.1:n.173+2006A>G
NM_001029883.3:c.3101T>C MANE Select NP_001025054.1:p.Val1034Ala