Canonical Allele Identifier: CA1241018999
Gene: PCARE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29073047G= , CM000664.2:g.29073047G= GRCh38
NC_000002.11:g.29295913G= , CM000664.1:g.29295913G= GRCh37
NC_000002.10:g.29149417G= NCBI36
NG_021427.1:g.6215C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1215C= MANE Select ENSP00000332809.4:p.Gly405=
ENST00000331664.5:c.1215C= ENSP00000332809.4:p.Gly405=
NM_001029883.2:c.1215C= NP_001025054.1:p.Gly405=
XM_011532826.1:c.1215C= XP_011531128.1:p.Gly405=
XR_939901.1:n.185+3880G=
XR_939902.1:n.173+3892G=
NM_001029883.3:c.1215C= MANE Select NP_001025054.1:p.Gly405=