Canonical Allele Identifier: CA1241017477
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070846G= , CM000664.2:g.29070846G= GRCh38
NC_000002.11:g.29293712G= , CM000664.1:g.29293712G= GRCh37
NC_000002.10:g.29147216G= NCBI36
NG_021427.1:g.8416C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3416C= MANE Select ENSP00000332809.4:p.Thr1139=
ENST00000331664.5:c.3416C= ENSP00000332809.4:p.Thr1139=
NM_001029883.2:c.3416C= NP_001025054.1:p.Thr1139=
XM_011532826.1:c.3416C= XP_011531128.1:p.Thr1139=
XR_939901.1:n.185+1679G=
XR_939902.1:n.173+1691G=
NM_001029883.3:c.3416C= MANE Select NP_001025054.1:p.Thr1139=
Search 100 bp 5'
Search 100 bp 3'