Canonical Allele Identifier: CA2211961395

Gene: PDILT

Linked Data

• dbSNP Id: rs1966575293

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20389111_20389135del , CM000678.2:g.20389111_20389135del	GRCh38
NC_000016.9:g.20400433_20400457del , CM000678.1:g.20400433_20400457del	GRCh37
NC_000016.8:g.20307934_20307958del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302451.9:c.203-4281_203-4257del MANE Select	ENSP00000305465.4:n.203-4281_203-4257del
ENST00000302451.8:c.203-4281_203-4257del	ENSP00000305465.4:n.203-4281_203-4257del
ENST00000575561.1:c.203-223_203-199del	ENSP00000459161.1:n.203-223_203-199del
NM_174924.1:c.203-4281_203-4257del	NP_777584.1:n.203-4281_203-4257del
XM_006721024.1:c.203-4281_203-4257del	XP_006721087.1:n.203-4281_203-4257del
XM_011545764.1:c.203-4281_203-4257del	XP_011544066.1:n.203-4281_203-4257del
XM_011545765.1:c.203-4281_203-4257del	XP_011544067.1:n.203-4281_203-4257del
XR_950754.1:n.457-4281_457-4257del
NM_174924.2:c.203-4281_203-4257del MANE Select	NP_777584.1:n.203-4281_203-4257del