Canonical Allele Identifier: CA718935102
Gene: PDILT HGNC NCBI

Linked Data

dbSNP Id: rs1350908547
MyVariant Identifiers: chr16:g.20400779del (hg19) chr16:g.20389457del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20389457del , CM000678.2:g.20389457del GRCh38
NC_000016.9:g.20400779del , CM000678.1:g.20400779del GRCh37
NC_000016.8:g.20308280del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302451.9:c.203-4606del MANE Select ENSP00000305465.4:n.203-4606del
ENST00000302451.8:c.203-4606del ENSP00000305465.4:n.203-4606del
ENST00000575561.1:c.203-548del ENSP00000459161.1:n.203-548del
NM_174924.1:c.203-4606del NP_777584.1:n.203-4606del
XM_006721024.1:c.203-4606del XP_006721087.1:n.203-4606del
XM_011545764.1:c.203-4606del XP_011544066.1:n.203-4606del
XM_011545765.1:c.203-4606del XP_011544067.1:n.203-4606del
XR_950754.1:n.457-4606del
NM_174924.2:c.203-4606del MANE Select NP_777584.1:n.203-4606del
Search 100 bp 5'
Search 100 bp 3'