Canonical Allele Identifier: CA4154501
Gene: DAGLB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6430575G>A , CM000669.2:g.6430575G>A GRCh38
NC_000007.13:g.6470206G>A , CM000669.1:g.6470206G>A GRCh37
NC_000007.12:g.6436731G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000297056.11:c.834C>T MANE Select ENSP00000297056.6:p.Cys278=
ENST00000297056.10:c.834C>T ENSP00000297056.6:p.Cys278=
ENST00000425398.6:c.542+2262C>T ENSP00000391171.2:n.542+2262C>T
ENST00000432248.1:c.420-4461C>T ENSP00000410787.1:n.420-4461C>T
ENST00000436575.5:c.711C>T ENSP00000404785.1:p.Cys237=
ENST00000454738.5:c.370+2262C>T ENSP00000411746.1:n.370+2262C>T
NM_001142936.1:c.542+2262C>T NP_001136408.1:n.542+2262C>T
NM_139179.3:c.834C>T NP_631918.3:p.Cys278=
NM_139179.4:c.834C>T MANE Select NP_631918.3:p.Cys278=
NM_001142936.2:c.542+2262C>T NP_001136408.1:n.542+2262C>T