Canonical Allele Identifier: CA2612741941

Gene: LDHA

Linked Data

• gnomAD v4: 11-18407134-GGAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407139_18407141del , CM000673.2:g.18407139_18407141del	GRCh38
NC_000011.9:g.18428686_18428688del , CM000673.1:g.18428686_18428688del	GRCh37
NC_000011.8:g.18385262_18385264del	NCBI36
NG_008185.1:g.17705_17707del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.857_859del MANE Select	ENSP00000395337.3:p.Asp286del
ENST00000227157.8:c.*7_*9del	ENSP00000227157.4:n.*7_*9del
ENST00000375710.7:n.1724_1726del
ENST00000379412.9:c.857_859del	ENSP00000368722.5:p.Asp286del
ENST00000396222.6:c.688-100_688-98del	ENSP00000379524.2:n.688-100_688-98del
ENST00000422447.7:c.857_859del	ENSP00000395337.3:p.Asp286del
ENST00000430553.6:c.683_685del	ENSP00000406172.2:p.Asp228del
ENST00000538451.1:n.744_746del
ENST00000540430.5:c.944_946del	ENSP00000445175.1:p.Asp315del
ENST00000541097.5:c.*195_*197del	ENSP00000443362.1:n.*195_*197del
ENST00000542179.1:c.857_859del	ENSP00000445331.1:p.Asp286del
ENST00000545215.5:c.*601_*603del	ENSP00000442637.1:n.*601_*603del
NM_001135239.1:c.683_685del	NP_001128711.1:p.Asp228del
NM_001165414.1:c.944_946del	NP_001158886.1:p.Asp315del
NM_001165415.1:c.688-100_688-98del	NP_001158887.1:n.688-100_688-98del
NM_001165416.1:c.*7_*9del	NP_001158888.1:n.*7_*9del
NM_005566.3:c.857_859del	NP_005557.1:p.Asp286del
NR_028500.1:n.1011_1013del
NM_005566.4:c.857_859del MANE Select	NP_005557.1:p.Asp286del
NM_001165415.2:c.688-100_688-98del	NP_001158887.1:n.688-100_688-98del
NM_001135239.2:c.683_685del	NP_001128711.1:p.Asp228del
NM_001165414.2:c.944_946del	NP_001158886.1:p.Asp315del
NM_001165416.2:c.*7_*9del	NP_001158888.1:n.*7_*9del
NR_028500.2:n.837_839del