Canonical Allele Identifier: CA6036741
Gene: DAGLA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61734879C>T , CM000673.2:g.61734879C>T GRCh38
NC_000011.9:g.61502351C>T , CM000673.1:g.61502351C>T GRCh37
NC_000011.8:g.61258927C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000257215.10:c.1005C>T MANE Select ENSP00000257215.5:p.Phe335=
ENST00000257215.9:c.1005C>T ENSP00000257215.5:p.Phe335=
ENST00000540717.1:c.*478C>T ENSP00000440264.1:n.*478C>T
NM_006133.2:c.1005C>T NP_006124.1:p.Phe335=
XM_005274230.3:c.1005C>T XP_005274287.1:p.Phe335=
XM_011545235.1:c.1005C>T XP_011543537.1:p.Phe335=
XM_011545236.1:c.1005C>T XP_011543538.1:p.Phe335=
XM_017018238.1:c.1083C>T XP_016873727.1:p.Phe361=
XM_017018239.1:c.1083C>T XP_016873728.1:p.Phe361=
XM_017018240.1:c.1083C>T XP_016873729.1:p.Phe361=
NM_006133.3:c.1005C>T MANE Select NP_006124.1:p.Phe335=