Canonical Allele Identifier: CA2572891937
Gene: PDILT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20389245del , CM000678.2:g.20389245del GRCh38
NC_000016.9:g.20400567del , CM000678.1:g.20400567del GRCh37
NC_000016.8:g.20308068del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302451.9:c.203-4394del MANE Select ENSP00000305465.4:n.203-4394del
ENST00000302451.8:c.203-4394del ENSP00000305465.4:n.203-4394del
ENST00000575561.1:c.203-336del ENSP00000459161.1:n.203-336del
NM_174924.1:c.203-4394del NP_777584.1:n.203-4394del
XM_006721024.1:c.203-4394del XP_006721087.1:n.203-4394del
XM_011545764.1:c.203-4394del XP_011544066.1:n.203-4394del
XM_011545765.1:c.203-4394del XP_011544067.1:n.203-4394del
XR_950754.1:n.457-4394del
NM_174924.2:c.203-4394del MANE Select NP_777584.1:n.203-4394del