Canonical Allele Identifier: CA13383974
Gene: DAGLA HGNC NCBI

Linked Data

dbSNP Id: rs4963243
gnomAD v2: 11-61494327-G-A
gnomAD v3: 11-61726855-G-A
gnomAD v4: 11-61726855-G-A
MyVariant Identifiers: chr11:g.61494327G>A (hg19) chr11:g.61726855G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61726855G>A , CM000673.2:g.61726855G>A GRCh38
NC_000011.9:g.61494327G>A , CM000673.1:g.61494327G>A GRCh37
NC_000011.8:g.61250903G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000257215.10:c.636+773G>A MANE Select ENSP00000257215.5:n.636+773G>A
ENST00000257215.9:c.636+773G>A ENSP00000257215.5:n.636+773G>A
ENST00000540717.1:c.*109+773G>A ENSP00000440264.1:n.*109+773G>A
NM_006133.2:c.636+773G>A NP_006124.1:n.636+773G>A
XM_005274230.3:c.636+773G>A XP_005274287.1:n.636+773G>A
XM_011545235.1:c.636+773G>A XP_011543537.1:n.636+773G>A
XM_011545236.1:c.636+773G>A XP_011543538.1:n.636+773G>A
XM_017018238.1:c.636+773G>A XP_016873727.1:n.636+773G>A
XM_017018239.1:c.636+773G>A XP_016873728.1:n.636+773G>A
XM_017018240.1:c.636+773G>A XP_016873729.1:n.636+773G>A
NM_006133.3:c.636+773G>A MANE Select NP_006124.1:n.636+773G>A
Search 100 bp 5'
Search 100 bp 3'