Canonical Allele Identifier: CA2211961558
Gene: PDILT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20389456_20389457delinsGA , CM000678.2:g.20389456_20389457delinsGA GRCh38
NC_000016.9:g.20400778_20400779delinsGA , CM000678.1:g.20400778_20400779delinsGA GRCh37
NC_000016.8:g.20308279_20308280delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302451.9:c.203-4606_203-4605delinsTC MANE Select ENSP00000305465.4:n.203-4606_203-4605deli...
ENST00000302451.8:c.203-4606_203-4605delinsTC ENSP00000305465.4:n.203-4606_203-4605deli...
ENST00000575561.1:c.203-548_203-547delinsTC ENSP00000459161.1:n.203-548_203-547delins...
NM_174924.1:c.203-4606_203-4605delinsTC NP_777584.1:n.203-4606_203-4605delinsTC
XM_006721024.1:c.203-4606_203-4605delinsTC XP_006721087.1:n.203-4606_203-4605delinsT...
XM_011545764.1:c.203-4606_203-4605delinsTC XP_011544066.1:n.203-4606_203-4605delinsT...
XM_011545765.1:c.203-4606_203-4605delinsTC XP_011544067.1:n.203-4606_203-4605delinsT...
XR_950754.1:n.457-4606_457-4605delinsTC
NM_174924.2:c.203-4606_203-4605delinsTC MANE Select NP_777584.1:n.203-4606_203-4605delinsTC