Canonical Allele Identifier: CA1241018958
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29072960G= , CM000664.2:g.29072960G= GRCh38
NC_000002.11:g.29295826G= , CM000664.1:g.29295826G= GRCh37
NC_000002.10:g.29149330G= NCBI36
NG_021427.1:g.6302C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1302C= MANE Select ENSP00000332809.4:p.Cys434=
ENST00000331664.5:c.1302C= ENSP00000332809.4:p.Cys434=
NM_001029883.2:c.1302C= NP_001025054.1:p.Cys434=
XM_011532826.1:c.1302C= XP_011531128.1:p.Cys434=
XR_939901.1:n.185+3793G=
XR_939902.1:n.173+3805G=
NM_001029883.3:c.1302C= MANE Select NP_001025054.1:p.Cys434=
Search 100 bp 5'
Search 100 bp 3'