Canonical Allele Identifier: CA1241017772
Gene: PCARE HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070995_29070998delinsTGGG , CM000664.2:g.29070995_29070998delinsTGGG GRCh38
NC_000002.11:g.29293861_29293864delinsTGGG , CM000664.1:g.29293861_29293864delinsTGGG GRCh37
NC_000002.10:g.29147365_29147368delinsTGGG NCBI36
NG_021427.1:g.8264_8267delinsCCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3264_3267delinsCCCA MANE Select ENSP00000332809.4:p.Ser1088=
ENST00000331664.5:c.3264_3267delinsCCCA ENSP00000332809.4:p.Ser1088=
NM_001029883.2:c.3264_3267delinsCCCA NP_001025054.1:p.Ser1088=
XM_011532826.1:c.3264_3267delinsCCCA XP_011531128.1:p.Ser1088=
XR_939901.1:n.185+1828_185+1831delinsTGGG
XR_939902.1:n.173+1840_173+1843delinsTGGG
NM_001029883.3:c.3264_3267delinsCCCA MANE Select NP_001025054.1:p.Ser1088=
Search 100 bp 5'
Search 100 bp 3'