Canonical Allele Identifier: CA2211961523
Gene: PDILT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20389383_20389384delinsGT , CM000678.2:g.20389383_20389384delinsGT GRCh38
NC_000016.9:g.20400705_20400706delinsGT , CM000678.1:g.20400705_20400706delinsGT GRCh37
NC_000016.8:g.20308206_20308207delinsGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302451.9:c.203-4533_203-4532delinsAC MANE Select ENSP00000305465.4:n.203-4533_203-4532delinsAC
ENST00000302451.8:c.203-4533_203-4532delinsAC ENSP00000305465.4:n.203-4533_203-4532delinsAC
ENST00000575561.1:c.203-475_203-474delinsAC ENSP00000459161.1:n.203-475_203-474delinsAC
NM_174924.1:c.203-4533_203-4532delinsAC NP_777584.1:n.203-4533_203-4532delinsAC
XM_006721024.1:c.203-4533_203-4532delinsAC XP_006721087.1:n.203-4533_203-4532delinsAC
XM_011545764.1:c.203-4533_203-4532delinsAC XP_011544066.1:n.203-4533_203-4532delinsAC
XM_011545765.1:c.203-4533_203-4532delinsAC XP_011544067.1:n.203-4533_203-4532delinsAC
XR_950754.1:n.457-4533_457-4532delinsAC
NM_174924.2:c.203-4533_203-4532delinsAC MANE Select NP_777584.1:n.203-4533_203-4532delinsAC