Canonical Allele Identifier: CA2211961507

Gene: PDILT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20389340_20389344delinsAATAG , CM000678.2:g.20389340_20389344delinsAATAG	GRCh38
NC_000016.9:g.20400662_20400666delinsAATAG , CM000678.1:g.20400662_20400666delinsAATAG	GRCh37
NC_000016.8:g.20308163_20308167delinsAATAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302451.9:c.203-4493_203-4489delinsCTATT MANE Select	ENSP00000305465.4:n.203-4493_203-4489delinsCTATT
ENST00000302451.8:c.203-4493_203-4489delinsCTATT	ENSP00000305465.4:n.203-4493_203-4489delinsCTATT
ENST00000575561.1:c.203-435_203-431delinsCTATT	ENSP00000459161.1:n.203-435_203-431delinsCTATT
NM_174924.1:c.203-4493_203-4489delinsCTATT	NP_777584.1:n.203-4493_203-4489delinsCTATT
XM_006721024.1:c.203-4493_203-4489delinsCTATT	XP_006721087.1:n.203-4493_203-4489delinsCTATT
XM_011545764.1:c.203-4493_203-4489delinsCTATT	XP_011544066.1:n.203-4493_203-4489delinsCTATT
XM_011545765.1:c.203-4493_203-4489delinsCTATT	XP_011544067.1:n.203-4493_203-4489delinsCTATT
XR_950754.1:n.457-4493_457-4489delinsCTATT
NM_174924.2:c.203-4493_203-4489delinsCTATT MANE Select	NP_777584.1:n.203-4493_203-4489delinsCTATT