Canonical Allele Identifier: CA916500195
Gene: PCARE HGNC NCBI

Linked Data

dbSNP Id: rs138020654
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070999del , CM000664.2:g.29070999del GRCh38
NC_000002.11:g.29293865del , CM000664.1:g.29293865del GRCh37
NC_000002.10:g.29147369del NCBI36
NG_021427.1:g.8266del

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3266del MANE Select ENSP00000332809.4:p.Pro1089HisfsTer24
ENST00000331664.5:c.3266del ENSP00000332809.4:p.Pro1089HisfsTer24
NM_001029883.2:c.3266del NP_001025054.1:p.Pro1089HisfsTer24
XM_011532826.1:c.3266del XP_011531128.1:p.Pro1089HisfsTer24
XR_939901.1:n.185+1832del
XR_939902.1:n.173+1844del
NM_001029883.3:c.3266del MANE Select NP_001025054.1:p.Pro1089HisfsTer24
Search 100 bp 5'
Search 100 bp 3'