Canonical Allele Identifier: CA2211965003
Gene: PDILT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20396961C= , CM000678.2:g.20396961C= GRCh38
NC_000016.9:g.20408283C= , CM000678.1:g.20408283C= GRCh37
NC_000016.8:g.20315784C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302451.9:c.202+2138G= MANE Select ENSP00000305465.4:n.202+2138G=
ENST00000302451.8:c.202+2138G= ENSP00000305465.4:n.202+2138G=
ENST00000575561.1:c.202+2138G= ENSP00000459161.1:n.202+2138G=
NM_174924.1:c.202+2138G= NP_777584.1:n.202+2138G=
XM_006721024.1:c.202+2138G= XP_006721087.1:n.202+2138G=
XM_011545764.1:c.202+2138G= XP_011544066.1:n.202+2138G=
XM_011545765.1:c.202+2138G= XP_011544067.1:n.202+2138G=
XR_950754.1:n.456+2138G=
NM_174924.2:c.202+2138G= MANE Select NP_777584.1:n.202+2138G=
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