Canonical Allele Identifier: CA1241017982
Gene: PCARE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071160C= , CM000664.2:g.29071160C= GRCh38
NC_000002.11:g.29294026C= , CM000664.1:g.29294026C= GRCh37
NC_000002.10:g.29147530C= NCBI36
NG_021427.1:g.8102G=

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3102G= MANE Select ENSP00000332809.4:p.Val1034=
ENST00000331664.5:c.3102G= ENSP00000332809.4:p.Val1034=
NM_001029883.2:c.3102G= NP_001025054.1:p.Val1034=
XM_011532826.1:c.3102G= XP_011531128.1:p.Val1034=
XR_939901.1:n.185+1993C=
XR_939902.1:n.173+2005C=
NM_001029883.3:c.3102G= MANE Select NP_001025054.1:p.Val1034=