Canonical Allele Identifier: CA2211961566
Gene: PDILT HGNC NCBI

Linked Data

dbSNP Id: rs1966581434

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20389478dup , CM000678.2:g.20389478dup GRCh38
NC_000016.9:g.20400800dup , CM000678.1:g.20400800dup GRCh37
NC_000016.8:g.20308301dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302451.9:c.203-4625dup MANE Select ENSP00000305465.4:n.203-4625dup
ENST00000302451.8:c.203-4625dup ENSP00000305465.4:n.203-4625dup
ENST00000575561.1:c.203-567dup ENSP00000459161.1:n.203-567dup
NM_174924.1:c.203-4625dup NP_777584.1:n.203-4625dup
XM_006721024.1:c.203-4625dup XP_006721087.1:n.203-4625dup
XM_011545764.1:c.203-4625dup XP_011544066.1:n.203-4625dup
XM_011545765.1:c.203-4625dup XP_011544067.1:n.203-4625dup
XR_950754.1:n.457-4625dup
NM_174924.2:c.203-4625dup MANE Select NP_777584.1:n.203-4625dup