Canonical Allele Identifier: CA346472841
Gene: PCARE HGNC NCBI

Linked Data

gnomAD v4: 2-29070669-T-C
COSMIC: COSM148823

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070669T>C , CM000664.2:g.29070669T>C GRCh38
NC_000002.11:g.29293535T>C , CM000664.1:g.29293535T>C GRCh37
NC_000002.10:g.29147039T>C NCBI36
NG_021427.1:g.8593A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3593A>G MANE Select ENSP00000332809.4:p.Gln1198Arg
ENST00000331664.5:c.3593A>G ENSP00000332809.4:p.Gln1198Arg
NM_001029883.2:c.3593A>G NP_001025054.1:p.Gln1198Arg
XM_011532826.1:c.3593A>G XP_011531128.1:p.Gln1198Arg
XR_939901.1:n.185+1502T>C
XR_939902.1:n.173+1514T>C
NM_001029883.3:c.3593A>G MANE Select NP_001025054.1:p.Gln1198Arg