Canonical Allele Identifier: CA346475591
Gene: PCARE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071053A>G , CM000664.2:g.29071053A>G GRCh38
NC_000002.11:g.29293919A>G , CM000664.1:g.29293919A>G GRCh37
NC_000002.10:g.29147423A>G NCBI36
NG_021427.1:g.8209T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3209T>C MANE Select ENSP00000332809.4:p.Val1070Ala
ENST00000331664.5:c.3209T>C ENSP00000332809.4:p.Val1070Ala
NM_001029883.2:c.3209T>C NP_001025054.1:p.Val1070Ala
XM_011532826.1:c.3209T>C XP_011531128.1:p.Val1070Ala
XR_939901.1:n.185+1886A>G
XR_939902.1:n.173+1898A>G
NM_001029883.3:c.3209T>C MANE Select NP_001025054.1:p.Val1070Ala