Canonical Allele Identifier: CA1028803797
Gene: PCARE HGNC NCBI

Linked Data

dbSNP Id: rs1667521360
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29073040_29073042del , CM000664.2:g.29073040_29073042del GRCh38
NC_000002.11:g.29295906_29295908del , CM000664.1:g.29295906_29295908del GRCh37
NC_000002.10:g.29149410_29149412del NCBI36
NG_021427.1:g.6221_6223del

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1221_1223del MANE Select ENSP00000332809.4:p.Arg408del
ENST00000331664.5:c.1221_1223del ENSP00000332809.4:p.Arg408del
NM_001029883.2:c.1221_1223del NP_001025054.1:p.Arg408del
XM_011532826.1:c.1221_1223del XP_011531128.1:p.Arg408del
XR_939901.1:n.185+3873_185+3875del
XR_939902.1:n.173+3885_173+3887del
NM_001029883.3:c.1221_1223del MANE Select NP_001025054.1:p.Arg408del
Search 100 bp 5'
Search 100 bp 3'