Canonical Allele Identifier: CA2211961567
Gene: PDILT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20389480G= , CM000678.2:g.20389480G= GRCh38
NC_000016.9:g.20400802G= , CM000678.1:g.20400802G= GRCh37
NC_000016.8:g.20308303G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302451.9:c.203-4629C= MANE Select ENSP00000305465.4:n.203-4629C=
ENST00000302451.8:c.203-4629C= ENSP00000305465.4:n.203-4629C=
ENST00000575561.1:c.203-571C= ENSP00000459161.1:n.203-571C=
NM_174924.1:c.203-4629C= NP_777584.1:n.203-4629C=
XM_006721024.1:c.203-4629C= XP_006721087.1:n.203-4629C=
XM_011545764.1:c.203-4629C= XP_011544066.1:n.203-4629C=
XM_011545765.1:c.203-4629C= XP_011544067.1:n.203-4629C=
XR_950754.1:n.457-4629C=
NM_174924.2:c.203-4629C= MANE Select NP_777584.1:n.203-4629C=