Canonical Allele Identifier: CA1241017475
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070837G= , CM000664.2:g.29070837G= GRCh38
NC_000002.11:g.29293703G= , CM000664.1:g.29293703G= GRCh37
NC_000002.10:g.29147207G= NCBI36
NG_021427.1:g.8425C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3425C= MANE Select ENSP00000332809.4:p.Pro1142=
ENST00000331664.5:c.3425C= ENSP00000332809.4:p.Pro1142=
NM_001029883.2:c.3425C= NP_001025054.1:p.Pro1142=
XM_011532826.1:c.3425C= XP_011531128.1:p.Pro1142=
XR_939901.1:n.185+1670G=
XR_939902.1:n.173+1682G=
NM_001029883.3:c.3425C= MANE Select NP_001025054.1:p.Pro1142=
Search 100 bp 5'
Search 100 bp 3'