Canonical Allele Identifier: CA2576924620
Gene: PCARE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071052del , CM000664.2:g.29071052del GRCh38
NC_000002.11:g.29293918del , CM000664.1:g.29293918del GRCh37
NC_000002.10:g.29147422del NCBI36
NG_021427.1:g.8213del

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3213del MANE Select ENSP00000332809.4:p.Ser1072AlafsTer?
ENST00000331664.5:c.3213del ENSP00000332809.4:p.Ser1072AlafsTer?
NM_001029883.2:c.3213del NP_001025054.1:p.Ser1072AlafsTer?
XM_011532826.1:c.3213del XP_011531128.1:p.Ser1072AlafsTer?
XR_939901.1:n.185+1885del
XR_939902.1:n.173+1897del
NM_001029883.3:c.3213del MANE Select NP_001025054.1:p.Ser1072AlafsTer?