Canonical Allele Identifier: CA2211965008
Gene: PDILT HGNC NCBI

Linked Data

dbSNP Id: rs1966669710

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20396974del , CM000678.2:g.20396974del GRCh38
NC_000016.9:g.20408296del , CM000678.1:g.20408296del GRCh37
NC_000016.8:g.20315797del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302451.9:c.202+2125del MANE Select ENSP00000305465.4:n.202+2125del
ENST00000302451.8:c.202+2125del ENSP00000305465.4:n.202+2125del
ENST00000575561.1:c.202+2125del ENSP00000459161.1:n.202+2125del
NM_174924.1:c.202+2125del NP_777584.1:n.202+2125del
XM_006721024.1:c.202+2125del XP_006721087.1:n.202+2125del
XM_011545764.1:c.202+2125del XP_011544066.1:n.202+2125del
XM_011545765.1:c.202+2125del XP_011544067.1:n.202+2125del
XR_950754.1:n.456+2125del
NM_174924.2:c.202+2125del MANE Select NP_777584.1:n.202+2125del