Canonical Allele Identifier: CA2612742074

Gene: LDHA

Linked Data

• gnomAD v4: 11-18407461-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407461T>C , CM000673.2:g.18407461T>C	GRCh38
NC_000011.9:g.18429008T>C , CM000673.1:g.18429008T>C	GRCh37
NC_000011.8:g.18385584T>C	NCBI36
NG_008185.1:g.18027T>C
NG_011816.1:g.156T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*180T>C MANE Select	ENSP00000395337.3:n.*180T>C
ENST00000227157.8:c.*329T>C	ENSP00000227157.4:n.*329T>C
ENST00000375710.7:n.2046T>C
ENST00000379412.9:c.*180T>C	ENSP00000368722.5:n.*180T>C
ENST00000396222.6:c.*85T>C	ENSP00000379524.2:n.*85T>C
ENST00000422447.7:c.*180T>C	ENSP00000395337.3:n.*180T>C
ENST00000430553.6:c.*180T>C	ENSP00000406172.2:n.*180T>C
ENST00000538451.1:n.1066T>C
ENST00000540430.5:c.*180T>C	ENSP00000445175.1:n.*180T>C
ENST00000545215.5:c.*923T>C	ENSP00000442637.1:n.*923T>C
NM_001135239.1:c.*180T>C	NP_001128711.1:n.*180T>C
NM_001165414.1:c.*180T>C	NP_001158886.1:n.*180T>C
NM_001165415.1:c.*85T>C	NP_001158887.1:n.*85T>C
NM_001165416.1:c.*329T>C	NP_001158888.1:n.*329T>C
NM_005566.3:c.*180T>C	NP_005557.1:n.*180T>C
NR_028500.1:n.1333T>C
NM_005566.4:c.*180T>C MANE Select	NP_005557.1:n.*180T>C
NM_001165415.2:c.*85T>C	NP_001158887.1:n.*85T>C
NM_001135239.2:c.*180T>C	NP_001128711.1:n.*180T>C
NM_001165414.2:c.*180T>C	NP_001158886.1:n.*180T>C
NM_001165416.2:c.*329T>C	NP_001158888.1:n.*329T>C
NR_028500.2:n.1159T>C