Canonical Allele Identifier: CA2211961669

Gene: PDILT

Linked Data

• dbSNP Id: rs1398036168

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20389672G>T , CM000678.2:g.20389672G>T	GRCh38
NC_000016.9:g.20400994G>T , CM000678.1:g.20400994G>T	GRCh37
NC_000016.8:g.20308495G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302451.9:c.203-4821C>A MANE Select	ENSP00000305465.4:n.203-4821C>A
ENST00000302451.8:c.203-4821C>A	ENSP00000305465.4:n.203-4821C>A
ENST00000575561.1:c.203-763C>A	ENSP00000459161.1:n.203-763C>A
NM_174924.1:c.203-4821C>A	NP_777584.1:n.203-4821C>A
XM_006721024.1:c.203-4821C>A	XP_006721087.1:n.203-4821C>A
XM_011545764.1:c.203-4821C>A	XP_011544066.1:n.203-4821C>A
XM_011545765.1:c.203-4821C>A	XP_011544067.1:n.203-4821C>A
XR_950754.1:n.457-4821C>A
NM_174924.2:c.203-4821C>A MANE Select	NP_777584.1:n.203-4821C>A