Canonical Allele Identifier: CA2535786490
Gene: PDILT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20389685_20389686insT , CM000678.2:g.20389685_20389686insT GRCh38
NC_000016.9:g.20401007_20401008insT , CM000678.1:g.20401007_20401008insT GRCh37
NC_000016.8:g.20308508_20308509insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302451.9:c.203-4835_203-4834insA MANE Select ENSP00000305465.4:n.203-4835_203-4834insA
ENST00000302451.8:c.203-4835_203-4834insA ENSP00000305465.4:n.203-4835_203-4834insA
ENST00000575561.1:c.203-777_203-776insA ENSP00000459161.1:n.203-777_203-776insA
NM_174924.1:c.203-4835_203-4834insA NP_777584.1:n.203-4835_203-4834insA
XM_006721024.1:c.203-4835_203-4834insA XP_006721087.1:n.203-4835_203-4834insA
XM_011545764.1:c.203-4835_203-4834insA XP_011544066.1:n.203-4835_203-4834insA
XM_011545765.1:c.203-4835_203-4834insA XP_011544067.1:n.203-4835_203-4834insA
XR_950754.1:n.457-4835_457-4834insA
NM_174924.2:c.203-4835_203-4834insA MANE Select NP_777584.1:n.203-4835_203-4834insA