Canonical Allele Identifier: CA2211961505
Gene: PDILT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20389339_20389340delinsTA , CM000678.2:g.20389339_20389340delinsTA GRCh38
NC_000016.9:g.20400661_20400662delinsTA , CM000678.1:g.20400661_20400662delinsTA GRCh37
NC_000016.8:g.20308162_20308163delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302451.9:c.203-4489_203-4488delinsTA MANE Select ENSP00000305465.4:n.203-4489_203-4488delinsTA
ENST00000302451.8:c.203-4489_203-4488delinsTA ENSP00000305465.4:n.203-4489_203-4488delinsTA
ENST00000575561.1:c.203-431_203-430delinsTA ENSP00000459161.1:n.203-431_203-430delinsTA
NM_174924.1:c.203-4489_203-4488delinsTA NP_777584.1:n.203-4489_203-4488delinsTA
XM_006721024.1:c.203-4489_203-4488delinsTA XP_006721087.1:n.203-4489_203-4488delinsTA
XM_011545764.1:c.203-4489_203-4488delinsTA XP_011544066.1:n.203-4489_203-4488delinsTA
XM_011545765.1:c.203-4489_203-4488delinsTA XP_011544067.1:n.203-4489_203-4488delinsTA
XR_950754.1:n.457-4489_457-4488delinsTA
NM_174924.2:c.203-4489_203-4488delinsTA MANE Select NP_777584.1:n.203-4489_203-4488delinsTA