Canonical Allele Identifier: CA379509239

Gene: LDHA

Linked Data

• MyVariant Identifiers: chr11:g.18428800G>T (hg19) ; chr11:g.18407253G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407253G>T , CM000673.2:g.18407253G>T	GRCh38
NC_000011.9:g.18428800G>T , CM000673.1:g.18428800G>T	GRCh37
NC_000011.8:g.18385376G>T	NCBI36
NG_008185.1:g.17819G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.971G>T MANE Select	ENSP00000395337.3:p.Trp324Leu
ENST00000227157.8:c.*121G>T	ENSP00000227157.4:n.*121G>T
ENST00000375710.7:n.1838G>T
ENST00000379412.9:c.971G>T	ENSP00000368722.5:p.Trp324Leu
ENST00000396222.6:c.702G>T	ENSP00000379524.2:p.Leu234Phe
ENST00000422447.7:c.971G>T	ENSP00000395337.3:p.Trp324Leu
ENST00000430553.6:c.797G>T	ENSP00000406172.2:p.Trp266Leu
ENST00000538451.1:n.858G>T
ENST00000540430.5:c.1058G>T	ENSP00000445175.1:p.Trp353Leu
ENST00000542179.1:c.971G>T	ENSP00000445331.1:p.Trp324Leu
ENST00000545215.5:c.*715G>T	ENSP00000442637.1:n.*715G>T
NM_001135239.1:c.797G>T	NP_001128711.1:p.Trp266Leu
NM_001165414.1:c.1058G>T	NP_001158886.1:p.Trp353Leu
NM_001165415.1:c.702G>T	NP_001158887.1:p.Leu234Phe
NM_001165416.1:c.*121G>T	NP_001158888.1:n.*121G>T
NM_005566.3:c.971G>T	NP_005557.1:p.Trp324Leu
NR_028500.1:n.1125G>T
NM_005566.4:c.971G>T MANE Select	NP_005557.1:p.Trp324Leu
NM_001165415.2:c.702G>T	NP_001158887.1:p.Leu234Phe
NM_001135239.2:c.797G>T	NP_001128711.1:p.Trp266Leu
NM_001165414.2:c.1058G>T	NP_001158886.1:p.Trp353Leu
NM_001165416.2:c.*121G>T	NP_001158888.1:n.*121G>T
NR_028500.2:n.951G>T