Canonical Allele Identifier: CA346475600
Gene: PCARE HGNC NCBI

Linked Data

gnomAD v4: 2-29071057-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071057T>G , CM000664.2:g.29071057T>G GRCh38
NC_000002.11:g.29293923T>G , CM000664.1:g.29293923T>G GRCh37
NC_000002.10:g.29147427T>G NCBI36
NG_021427.1:g.8205A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3205A>C MANE Select ENSP00000332809.4:p.Lys1069Gln
ENST00000331664.5:c.3205A>C ENSP00000332809.4:p.Lys1069Gln
NM_001029883.2:c.3205A>C NP_001025054.1:p.Lys1069Gln
XM_011532826.1:c.3205A>C XP_011531128.1:p.Lys1069Gln
XR_939901.1:n.185+1890T>G
XR_939902.1:n.173+1902T>G
NM_001029883.3:c.3205A>C MANE Select NP_001025054.1:p.Lys1069Gln