Canonical Allele Identifier: CA2211961513
Gene: PDILT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20389352_20389353delinsGT , CM000678.2:g.20389352_20389353delinsGT GRCh38
NC_000016.9:g.20400674_20400675delinsGT , CM000678.1:g.20400674_20400675delinsGT GRCh37
NC_000016.8:g.20308175_20308176delinsGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302451.9:c.203-4502_203-4501delinsAC MANE Select ENSP00000305465.4:n.203-4502_203-4501delinsAC
ENST00000302451.8:c.203-4502_203-4501delinsAC ENSP00000305465.4:n.203-4502_203-4501delinsAC
ENST00000575561.1:c.203-444_203-443delinsAC ENSP00000459161.1:n.203-444_203-443delinsAC
NM_174924.1:c.203-4502_203-4501delinsAC NP_777584.1:n.203-4502_203-4501delinsAC
XM_006721024.1:c.203-4502_203-4501delinsAC XP_006721087.1:n.203-4502_203-4501delinsAC
XM_011545764.1:c.203-4502_203-4501delinsAC XP_011544066.1:n.203-4502_203-4501delinsAC
XM_011545765.1:c.203-4502_203-4501delinsAC XP_011544067.1:n.203-4502_203-4501delinsAC
XR_950754.1:n.457-4502_457-4501delinsAC
NM_174924.2:c.203-4502_203-4501delinsAC MANE Select NP_777584.1:n.203-4502_203-4501delinsAC