Canonical Allele Identifier: CA1732860020
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917257_107917266delinsTTGATTTCTG , CM000669.2:g.107917257_107917266delinsTTGATTTCTG GRCh38
NC_000007.13:g.107557702_107557711delinsTTGATTTCTG , CM000669.1:g.107557702_107557711delinsTTGATTTCTG GRCh37
NC_000007.12:g.107344938_107344947delinsTTGATTTCTG NCBI36
NG_008045.1:g.31117_31126delinsTTGATTTCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1047-16_1047-7delinsTTGATTTCTG MANE Select ENSP00000205402.3:n.1047-16_1047-7delinsTTGATTTCTG
ENST00000205402.9:c.1047-16_1047-7delinsTTGATTTCTG ENSP00000205402.3:n.1047-16_1047-7delinsTTGATTTCTG
ENST00000415325.5:c.*721-16_*721-7delinsTTGATTTCTG ENSP00000402593.1:n.*721-16_*721-7delinsTTGATTTCTG
ENST00000417551.5:c.1047-16_1047-7delinsTTGATTTCTG ENSP00000390667.1:n.1047-16_1047-7delinsTTGATTTCTG
ENST00000437604.6:c.903-16_903-7delinsTTGATTTCTG ENSP00000387542.2:n.903-16_903-7delinsTTGATTTCTG
ENST00000440410.5:c.978-16_978-7delinsTTGATTTCTG ENSP00000417016.1:n.978-16_978-7delinsTTGATTTCTG
NM_000108.4:c.1047-16_1047-7delinsTTGATTTCTG NP_000099.2:n.1047-16_1047-7delinsTTGATTTCTG
NM_001289750.1:c.750-16_750-7delinsTTGATTTCTG NP_001276679.1:n.750-16_750-7delinsTTGATTTCTG
NM_001289751.1:c.978-16_978-7delinsTTGATTTCTG NP_001276680.1:n.978-16_978-7delinsTTGATTTCTG
NM_001289752.1:c.903-16_903-7delinsTTGATTTCTG NP_001276681.1:n.903-16_903-7delinsTTGATTTCTG
NM_000108.5:c.1047-16_1047-7delinsTTGATTTCTG MANE Select NP_000099.2:n.1047-16_1047-7delinsTTGATTTCTG