Canonical Allele Identifier: CA379508698

Gene: LDHA

Linked Data

• gnomAD v3: 11-18407141-G-T
• gnomAD v4: 11-18407141-G-T
• MyVariant Identifiers: chr11:g.18428688G>T (hg19) ; chr11:g.18407141G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407141G>T , CM000673.2:g.18407141G>T	GRCh38
NC_000011.9:g.18428688G>T , CM000673.1:g.18428688G>T	GRCh37
NC_000011.8:g.18385264G>T	NCBI36
NG_008185.1:g.17707G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.859G>T MANE Select	ENSP00000395337.3:p.Val287Phe
ENST00000227157.8:c.*9G>T	ENSP00000227157.4:n.*9G>T
ENST00000375710.7:n.1726G>T
ENST00000379412.9:c.859G>T	ENSP00000368722.5:p.Val287Phe
ENST00000396222.6:c.688-98G>T	ENSP00000379524.2:n.688-98G>T
ENST00000422447.7:c.859G>T	ENSP00000395337.3:p.Val287Phe
ENST00000430553.6:c.685G>T	ENSP00000406172.2:p.Val229Phe
ENST00000538451.1:n.746G>T
ENST00000540430.5:c.946G>T	ENSP00000445175.1:p.Val316Phe
ENST00000541097.5:c.*197G>T	ENSP00000443362.1:n.*197G>T
ENST00000542179.1:c.859G>T	ENSP00000445331.1:p.Val287Phe
ENST00000545215.5:c.*603G>T	ENSP00000442637.1:n.*603G>T
NM_001135239.1:c.685G>T	NP_001128711.1:p.Val229Phe
NM_001165414.1:c.946G>T	NP_001158886.1:p.Val316Phe
NM_001165415.1:c.688-98G>T	NP_001158887.1:n.688-98G>T
NM_001165416.1:c.*9G>T	NP_001158888.1:n.*9G>T
NM_005566.3:c.859G>T	NP_005557.1:p.Val287Phe
NR_028500.1:n.1013G>T
NM_005566.4:c.859G>T MANE Select	NP_005557.1:p.Val287Phe
NM_001165415.2:c.688-98G>T	NP_001158887.1:n.688-98G>T
NM_001135239.2:c.685G>T	NP_001128711.1:p.Val229Phe
NM_001165414.2:c.946G>T	NP_001158886.1:p.Val316Phe
NM_001165416.2:c.*9G>T	NP_001158888.1:n.*9G>T
NR_028500.2:n.839G>T