Canonical Allele Identifier: CA1241017517
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070861T= , CM000664.2:g.29070861T= GRCh38
NC_000002.11:g.29293727T= , CM000664.1:g.29293727T= GRCh37
NC_000002.10:g.29147231T= NCBI36
NG_021427.1:g.8401A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3401A= MANE Select ENSP00000332809.4:p.Lys1134=
ENST00000331664.5:c.3401A= ENSP00000332809.4:p.Lys1134=
NM_001029883.2:c.3401A= NP_001025054.1:p.Lys1134=
XM_011532826.1:c.3401A= XP_011531128.1:p.Lys1134=
XR_939901.1:n.185+1694T=
XR_939902.1:n.173+1706T=
NM_001029883.3:c.3401A= MANE Select NP_001025054.1:p.Lys1134=
Search 100 bp 5'
Search 100 bp 3'