Canonical Allele Identifier: CA1241018054
Gene: PCARE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071281G= , CM000664.2:g.29071281G= GRCh38
NC_000002.11:g.29294147G= , CM000664.1:g.29294147G= GRCh37
NC_000002.10:g.29147651G= NCBI36
NG_021427.1:g.7981C=

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.2981C= MANE Select ENSP00000332809.4:p.Ala994=
ENST00000331664.5:c.2981C= ENSP00000332809.4:p.Ala994=
NM_001029883.2:c.2981C= NP_001025054.1:p.Ala994=
XM_011532826.1:c.2981C= XP_011531128.1:p.Ala994=
XR_939901.1:n.185+2114G=
XR_939902.1:n.173+2126G=
NM_001029883.3:c.2981C= MANE Select NP_001025054.1:p.Ala994=