Canonical Allele Identifier: CA1241017259
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070749C= , CM000664.2:g.29070749C= GRCh38
NC_000002.11:g.29293615C= , CM000664.1:g.29293615C= GRCh37
NC_000002.10:g.29147119C= NCBI36
NG_021427.1:g.8513G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3513G= MANE Select ENSP00000332809.4:p.Leu1171=
ENST00000331664.5:c.3513G= ENSP00000332809.4:p.Leu1171=
NM_001029883.2:c.3513G= NP_001025054.1:p.Leu1171=
XM_011532826.1:c.3513G= XP_011531128.1:p.Leu1171=
XR_939901.1:n.185+1582C=
XR_939902.1:n.173+1594C=
NM_001029883.3:c.3513G= MANE Select NP_001025054.1:p.Leu1171=
Search 100 bp 5'
Search 100 bp 3'