Canonical Allele Identifier: CA2658449486
Gene: PCARE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071039_29071051del , CM000664.2:g.29071039_29071051del GRCh38
NC_000002.11:g.29293905_29293917del , CM000664.1:g.29293905_29293917del GRCh37
NC_000002.10:g.29147409_29147421del NCBI36
NG_021427.1:g.8217_8229del

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3217_3229del MANE Select ENSP00000332809.4:p.Pro1073ThrfsTer?
ENST00000331664.5:c.3217_3229del ENSP00000332809.4:p.Pro1073ThrfsTer?
NM_001029883.2:c.3217_3229del NP_001025054.1:p.Pro1073ThrfsTer?
XM_011532826.1:c.3217_3229del XP_011531128.1:p.Pro1073ThrfsTer?
XR_939901.1:n.185+1872_185+1884del
XR_939902.1:n.173+1884_173+1896del
NM_001029883.3:c.3217_3229del MANE Select NP_001025054.1:p.Pro1073ThrfsTer?