Canonical Allele Identifier: CA1241018992
Gene: PCARE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29073031C= , CM000664.2:g.29073031C= GRCh38
NC_000002.11:g.29295897C= , CM000664.1:g.29295897C= GRCh37
NC_000002.10:g.29149401C= NCBI36
NG_021427.1:g.6231G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1231G= MANE Select ENSP00000332809.4:p.Asp411=
ENST00000331664.5:c.1231G= ENSP00000332809.4:p.Asp411=
NM_001029883.2:c.1231G= NP_001025054.1:p.Asp411=
XM_011532826.1:c.1231G= XP_011531128.1:p.Asp411=
XR_939901.1:n.185+3864C=
XR_939902.1:n.173+3876C=
NM_001029883.3:c.1231G= MANE Select NP_001025054.1:p.Asp411=