Canonical Allele Identifier: CA1241017790
Gene: PCARE HGNC NCBI

Linked Data

dbSNP Id: rs1667466687
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070996_29070999del , CM000664.2:g.29070996_29070999del GRCh38
NC_000002.11:g.29293862_29293865del , CM000664.1:g.29293862_29293865del GRCh37
NC_000002.10:g.29147366_29147369del NCBI36
NG_021427.1:g.8263_8266del

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3263_3266del MANE Select ENSP00000332809.4:p.Ser1088TyrfsTer24
ENST00000331664.5:c.3263_3266del ENSP00000332809.4:p.Ser1088TyrfsTer24
NM_001029883.2:c.3263_3266del NP_001025054.1:p.Ser1088TyrfsTer24
XM_011532826.1:c.3263_3266del XP_011531128.1:p.Ser1088TyrfsTer24
XR_939901.1:n.185+1829_185+1832del
XR_939902.1:n.173+1841_173+1844del
NM_001029883.3:c.3263_3266del MANE Select NP_001025054.1:p.Ser1088TyrfsTer24
Search 100 bp 5'
Search 100 bp 3'