Canonical Allele Identifier: CA1241018008
Gene: PCARE HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071203_29071204delinsTG , CM000664.2:g.29071203_29071204delinsTG GRCh38
NC_000002.11:g.29294069_29294070delinsTG , CM000664.1:g.29294069_29294070delinsTG GRCh37
NC_000002.10:g.29147573_29147574delinsTG NCBI36
NG_021427.1:g.8058_8059delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3058_3059delinsCA MANE Select ENSP00000332809.4:p.Gln1020=
ENST00000331664.5:c.3058_3059delinsCA ENSP00000332809.4:p.Gln1020=
NM_001029883.2:c.3058_3059delinsCA NP_001025054.1:p.Gln1020=
XM_011532826.1:c.3058_3059delinsCA XP_011531128.1:p.Gln1020=
XR_939901.1:n.185+2036_185+2037delinsTG
XR_939902.1:n.173+2048_173+2049delinsTG
NM_001029883.3:c.3058_3059delinsCA MANE Select NP_001025054.1:p.Gln1020=
Search 100 bp 5'
Search 100 bp 3'