Canonical Allele Identifier: CA2525849261
Gene: PCARE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071053_29071085del , CM000664.2:g.29071053_29071085del GRCh38
NC_000002.11:g.29293919_29293951del , CM000664.1:g.29293919_29293951del GRCh37
NC_000002.10:g.29147423_29147455del NCBI36
NG_021427.1:g.8177_8209del

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3177_3209del MANE Select ENSP00000332809.4:p.Pro1060_Val1070del
ENST00000331664.5:c.3177_3209del ENSP00000332809.4:p.Pro1060_Val1070del
NM_001029883.2:c.3177_3209del NP_001025054.1:p.Pro1060_Val1070del
XM_011532826.1:c.3177_3209del XP_011531128.1:p.Pro1060_Val1070del
XR_939901.1:n.185+1886_185+1918del
XR_939902.1:n.173+1898_173+1930del
NM_001029883.3:c.3177_3209del MANE Select NP_001025054.1:p.Pro1060_Val1070del