Canonical Allele Identifier: CA2211961548
Gene: PDILT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20389430_20389431delinsAG , CM000678.2:g.20389430_20389431delinsAG GRCh38
NC_000016.9:g.20400752_20400753delinsAG , CM000678.1:g.20400752_20400753delinsAG GRCh37
NC_000016.8:g.20308253_20308254delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302451.9:c.203-4580_203-4579delinsCT MANE Select ENSP00000305465.4:n.203-4580_203-4579deli...
ENST00000302451.8:c.203-4580_203-4579delinsCT ENSP00000305465.4:n.203-4580_203-4579deli...
ENST00000575561.1:c.203-522_203-521delinsCT ENSP00000459161.1:n.203-522_203-521delins...
NM_174924.1:c.203-4580_203-4579delinsCT NP_777584.1:n.203-4580_203-4579delinsCT
XM_006721024.1:c.203-4580_203-4579delinsCT XP_006721087.1:n.203-4580_203-4579delinsC...
XM_011545764.1:c.203-4580_203-4579delinsCT XP_011544066.1:n.203-4580_203-4579delinsC...
XM_011545765.1:c.203-4580_203-4579delinsCT XP_011544067.1:n.203-4580_203-4579delinsC...
XR_950754.1:n.457-4580_457-4579delinsCT
NM_174924.2:c.203-4580_203-4579delinsCT MANE Select NP_777584.1:n.203-4580_203-4579delinsCT