Canonical Allele Identifier: CA4154711
Gene: DAGLB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6436388G>A , CM000669.2:g.6436388G>A GRCh38
NC_000007.13:g.6476019G>A , CM000669.1:g.6476019G>A GRCh37
NC_000007.12:g.6442544G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000297056.11:c.393C>T MANE Select ENSP00000297056.6:p.Asn131=
ENST00000297056.10:c.393C>T ENSP00000297056.6:p.Asn131=
ENST00000425398.6:c.393C>T ENSP00000391171.2:p.Asn131=
ENST00000432248.1:c.393C>T ENSP00000410787.1:p.Asn131=
ENST00000436575.5:c.270C>T ENSP00000404785.1:p.Asn90=
ENST00000454738.5:c.248-3429C>T ENSP00000411746.1:n.248-3429C>T
ENST00000479922.6:n.483C>T
NM_001142936.1:c.393C>T NP_001136408.1:p.Asn131=
NM_139179.3:c.393C>T NP_631918.3:p.Asn131=
NM_139179.4:c.393C>T MANE Select NP_631918.3:p.Asn131=
NM_001142936.2:c.393C>T NP_001136408.1:p.Asn131=