Canonical Allele Identifier: CA1241017919
Gene: PCARE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071052G= , CM000664.2:g.29071052G= GRCh38
NC_000002.11:g.29293918G= , CM000664.1:g.29293918G= GRCh37
NC_000002.10:g.29147422G= NCBI36
NG_021427.1:g.8210C=

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3210C= MANE Select ENSP00000332809.4:p.Val1070=
ENST00000331664.5:c.3210C= ENSP00000332809.4:p.Val1070=
NM_001029883.2:c.3210C= NP_001025054.1:p.Val1070=
XM_011532826.1:c.3210C= XP_011531128.1:p.Val1070=
XR_939901.1:n.185+1885G=
XR_939902.1:n.173+1897G=
NM_001029883.3:c.3210C= MANE Select NP_001025054.1:p.Val1070=