Canonical Allele Identifier: CA1955586596

Gene: LDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407201_18407203delinsACT , CM000673.2:g.18407201_18407203delinsACT	GRCh38
NC_000011.9:g.18428748_18428750delinsACT , CM000673.1:g.18428748_18428750delinsACT	GRCh37
NC_000011.8:g.18385324_18385326delinsACT	NCBI36
NG_008185.1:g.17767_17769delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.919_921delinsACT MANE Select	ENSP00000395337.3:p.Thr307=
ENST00000227157.8:c.*69_*71delinsACT	ENSP00000227157.4:n.*69_*71delinsACT
ENST00000375710.7:n.1786_1788delinsACT
ENST00000379412.9:c.919_921delinsACT	ENSP00000368722.5:p.Thr307=
ENST00000396222.6:c.688-38_688-36delinsACT	ENSP00000379524.2:n.688-38_688-36delinsACT
ENST00000422447.7:c.919_921delinsACT	ENSP00000395337.3:p.Thr307=
ENST00000430553.6:c.745_747delinsACT	ENSP00000406172.2:p.Thr249=
ENST00000538451.1:n.806_808delinsACT
ENST00000540430.5:c.1006_1008delinsACT	ENSP00000445175.1:p.Thr336=
ENST00000542179.1:c.919_921delinsACT	ENSP00000445331.1:p.Thr307=
ENST00000545215.5:c.*663_*665delinsACT	ENSP00000442637.1:n.*663_*665delinsACT
NM_001135239.1:c.745_747delinsACT	NP_001128711.1:p.Thr249=
NM_001165414.1:c.1006_1008delinsACT	NP_001158886.1:p.Thr336=
NM_001165415.1:c.688-38_688-36delinsACT	NP_001158887.1:n.688-38_688-36delinsACT
NM_001165416.1:c.*69_*71delinsACT	NP_001158888.1:n.*69_*71delinsACT
NM_005566.3:c.919_921delinsACT	NP_005557.1:p.Thr307=
NR_028500.1:n.1073_1075delinsACT
NM_005566.4:c.919_921delinsACT MANE Select	NP_005557.1:p.Thr307=
NM_001165415.2:c.688-38_688-36delinsACT	NP_001158887.1:n.688-38_688-36delinsACT
NM_001135239.2:c.745_747delinsACT	NP_001128711.1:p.Thr249=
NM_001165414.2:c.1006_1008delinsACT	NP_001158886.1:p.Thr336=
NM_001165416.2:c.*69_*71delinsACT	NP_001158888.1:n.*69_*71delinsACT
NR_028500.2:n.899_901delinsACT