Canonical Allele Identifier: CA2749314508
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071022_29071023insA , CM000664.2:g.29071022_29071023insA GRCh38
NC_000002.11:g.29293888_29293889insA , CM000664.1:g.29293888_29293889insA GRCh37
NC_000002.10:g.29147392_29147393insA NCBI36
NG_021427.1:g.8239_8240insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3239_3240insT MANE Select ENSP00000332809.4:p.Ser1081LysfsTer26
ENST00000331664.5:c.3239_3240insT ENSP00000332809.4:p.Ser1081LysfsTer26
NM_001029883.2:c.3239_3240insT NP_001025054.1:p.Ser1081LysfsTer26
XM_011532826.1:c.3239_3240insT XP_011531128.1:p.Ser1081LysfsTer26
XR_939901.1:n.185+1855_185+1856insA
XR_939902.1:n.173+1867_173+1868insA
NM_001029883.3:c.3239_3240insT MANE Select NP_001025054.1:p.Ser1081LysfsTer26
Search 100 bp 5'
Search 100 bp 3'