Canonical Allele Identifier: CA248519392

Gene: DGKH

Linked Data

• dbSNP Id: rs751642193
• gnomAD v2: 13-42653443-A-G
• gnomAD v3: 13-42079307-A-G
• gnomAD v4: 13-42079307-A-G
• MyVariant Identifiers: chr13:g.42653443A>G (hg19) ; chr13:g.42079307A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42079307A>G , CM000675.2:g.42079307A>G	GRCh38
NC_000013.10:g.42653443A>G , CM000675.1:g.42653443A>G	GRCh37
NC_000013.9:g.41551443A>G	NCBI36
NG_029191.2:g.44272A>G
NG_029191.3:g.44272A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000337343.9:c.192+30342A>G MANE Select	ENSP00000337572.4:n.192+30342A>G
ENST00000261491.9:c.192+30342A>G	ENSP00000261491.4:n.192+30342A>G
ENST00000337343.8:c.192+30342A>G	ENSP00000337572.4:n.192+30342A>G
ENST00000379274.6:c.192+30342A>G	ENSP00000368576.3:n.192+30342A>G
NM_001204504.2:c.192+30342A>G	NP_001191433.1:n.192+30342A>G
NM_152910.5:c.192+30342A>G	NP_690874.2:n.192+30342A>G
NM_178009.4:c.192+30342A>G	NP_821077.1:n.192+30342A>G
NM_152910.6:c.192+30342A>G	NP_690874.2:n.192+30342A>G
NM_178009.5:c.192+30342A>G MANE Select	NP_821077.1:n.192+30342A>G
NM_001204504.3:c.192+30342A>G	NP_001191433.1:n.192+30342A>G