Canonical Allele Identifier: CA718935072
Gene: PDILT HGNC NCBI

Linked Data

dbSNP Id: rs1490677439

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20389431G>A , CM000678.2:g.20389431G>A GRCh38
NC_000016.9:g.20400753G>A , CM000678.1:g.20400753G>A GRCh37
NC_000016.8:g.20308254G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302451.9:c.203-4580C>T MANE Select ENSP00000305465.4:n.203-4580C>T
ENST00000302451.8:c.203-4580C>T ENSP00000305465.4:n.203-4580C>T
ENST00000575561.1:c.203-522C>T ENSP00000459161.1:n.203-522C>T
NM_174924.1:c.203-4580C>T NP_777584.1:n.203-4580C>T
XM_006721024.1:c.203-4580C>T XP_006721087.1:n.203-4580C>T
XM_011545764.1:c.203-4580C>T XP_011544066.1:n.203-4580C>T
XM_011545765.1:c.203-4580C>T XP_011544067.1:n.203-4580C>T
XR_950754.1:n.457-4580C>T
NM_174924.2:c.203-4580C>T MANE Select NP_777584.1:n.203-4580C>T