Canonical Allele Identifier: CA1241017997
Gene: PCARE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071186C= , CM000664.2:g.29071186C= GRCh38
NC_000002.11:g.29294052C= , CM000664.1:g.29294052C= GRCh37
NC_000002.10:g.29147556C= NCBI36
NG_021427.1:g.8076G=

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3076G= MANE Select ENSP00000332809.4:p.Val1026=
ENST00000331664.5:c.3076G= ENSP00000332809.4:p.Val1026=
NM_001029883.2:c.3076G= NP_001025054.1:p.Val1026=
XM_011532826.1:c.3076G= XP_011531128.1:p.Val1026=
XR_939901.1:n.185+2019C=
XR_939902.1:n.173+2031C=
NM_001029883.3:c.3076G= MANE Select NP_001025054.1:p.Val1026=