Canonical Allele Identifier: CA2543182836
Gene: PDILT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20389688_20389689insACAGAGACAGACAGAGAAAGA , CM000678.2:g.20389688_20389689insACAGAGACAGACAGAGAAAGA GRCh38
NC_000016.9:g.20401010_20401011insACAGAGACAGACAGAGAAAGA , CM000678.1:g.20401010_20401011insACAGAGACAGACAGAGAAAGA GRCh37
NC_000016.8:g.20308511_20308512insACAGAGACAGACAGAGAAAGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302451.9:c.203-4838_203-4837insTCTTTCTCTGTCTGTCTCTGT MANE Select ENSP00000305465.4:n.203-4838_203-4837insTCTTTCTCTGTCTGTCTCTGT...
ENST00000302451.8:c.203-4838_203-4837insTCTTTCTCTGTCTGTCTCTGT ENSP00000305465.4:n.203-4838_203-4837insTCTTTCTCTGTCTGTCTCTGT...
ENST00000575561.1:c.203-780_203-779insTCTTTCTCTGTCTGTCTCTGT ENSP00000459161.1:n.203-780_203-779insTCTTTCTCTGTCTGTCTCTGT
NM_174924.1:c.203-4838_203-4837insTCTTTCTCTGTCTGTCTCTGT NP_777584.1:n.203-4838_203-4837insTCTTTCTCTGTCTGTCTCTGT
XM_006721024.1:c.203-4838_203-4837insTCTTTCTCTGTCTGTCTCTGT XP_006721087.1:n.203-4838_203-4837insTCTTTCTCTGTCTGTCTCTGT
XM_011545764.1:c.203-4838_203-4837insTCTTTCTCTGTCTGTCTCTGT XP_011544066.1:n.203-4838_203-4837insTCTTTCTCTGTCTGTCTCTGT
XM_011545765.1:c.203-4838_203-4837insTCTTTCTCTGTCTGTCTCTGT XP_011544067.1:n.203-4838_203-4837insTCTTTCTCTGTCTGTCTCTGT
XR_950754.1:n.457-4838_457-4837insTCTTTCTCTGTCTGTCTCTGT
NM_174924.2:c.203-4838_203-4837insTCTTTCTCTGTCTGTCTCTGT MANE Select NP_777584.1:n.203-4838_203-4837insTCTTTCTCTGTCTGTCTCTGT