Canonical Allele Identifier: CA2576924632
Gene: PCARE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29073037dup , CM000664.2:g.29073037dup GRCh38
NC_000002.11:g.29295903dup , CM000664.1:g.29295903dup GRCh37
NC_000002.10:g.29149407dup NCBI36
NG_021427.1:g.6228dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1228dup MANE Select ENSP00000332809.4:p.Gln410ProfsTer?
ENST00000331664.5:c.1228dup ENSP00000332809.4:p.Gln410ProfsTer?
NM_001029883.2:c.1228dup NP_001025054.1:p.Gln410ProfsTer?
XM_011532826.1:c.1228dup XP_011531128.1:p.Gln410ProfsTer?
XR_939901.1:n.185+3870dup
XR_939902.1:n.173+3882dup
NM_001029883.3:c.1228dup MANE Select NP_001025054.1:p.Gln410ProfsTer?