Canonical Allele Identifier: CA2211961439
Gene: PDILT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20389214C= , CM000678.2:g.20389214C= GRCh38
NC_000016.9:g.20400536C= , CM000678.1:g.20400536C= GRCh37
NC_000016.8:g.20308037C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302451.9:c.203-4363G= MANE Select ENSP00000305465.4:n.203-4363G=
ENST00000302451.8:c.203-4363G= ENSP00000305465.4:n.203-4363G=
ENST00000575561.1:c.203-305G= ENSP00000459161.1:n.203-305G=
NM_174924.1:c.203-4363G= NP_777584.1:n.203-4363G=
XM_006721024.1:c.203-4363G= XP_006721087.1:n.203-4363G=
XM_011545764.1:c.203-4363G= XP_011544066.1:n.203-4363G=
XM_011545765.1:c.203-4363G= XP_011544067.1:n.203-4363G=
XR_950754.1:n.457-4363G=
NM_174924.2:c.203-4363G= MANE Select NP_777584.1:n.203-4363G=
Search 100 bp 5'
Search 100 bp 3'