Canonical Allele Identifier: CA1241017921
Gene: PCARE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071054C= , CM000664.2:g.29071054C= GRCh38
NC_000002.11:g.29293920C= , CM000664.1:g.29293920C= GRCh37
NC_000002.10:g.29147424C= NCBI36
NG_021427.1:g.8208G=

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3208G= MANE Select ENSP00000332809.4:p.Val1070=
ENST00000331664.5:c.3208G= ENSP00000332809.4:p.Val1070=
NM_001029883.2:c.3208G= NP_001025054.1:p.Val1070=
XM_011532826.1:c.3208G= XP_011531128.1:p.Val1070=
XR_939901.1:n.185+1887C=
XR_939902.1:n.173+1899C=
NM_001029883.3:c.3208G= MANE Select NP_001025054.1:p.Val1070=