Canonical Allele Identifier: CA2612742096

Gene: LDHA

Linked Data

• gnomAD v4: 11-18407475-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407475G>T , CM000673.2:g.18407475G>T	GRCh38
NC_000011.9:g.18429022G>T , CM000673.1:g.18429022G>T	GRCh37
NC_000011.8:g.18385598G>T	NCBI36
NG_008185.1:g.18041G>T
NG_011816.1:g.170G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*194G>T MANE Select	ENSP00000395337.3:n.*194G>T
ENST00000227157.8:c.*343G>T	ENSP00000227157.4:n.*343G>T
ENST00000375710.7:n.2060G>T
ENST00000379412.9:c.*194G>T	ENSP00000368722.5:n.*194G>T
ENST00000396222.6:c.*99G>T	ENSP00000379524.2:n.*99G>T
ENST00000422447.7:c.*194G>T	ENSP00000395337.3:n.*194G>T
ENST00000430553.6:c.*194G>T	ENSP00000406172.2:n.*194G>T
ENST00000538451.1:n.1080G>T
ENST00000540430.5:c.*194G>T	ENSP00000445175.1:n.*194G>T
ENST00000545215.5:c.*937G>T	ENSP00000442637.1:n.*937G>T
NM_001135239.1:c.*194G>T	NP_001128711.1:n.*194G>T
NM_001165414.1:c.*194G>T	NP_001158886.1:n.*194G>T
NM_001165415.1:c.*99G>T	NP_001158887.1:n.*99G>T
NM_001165416.1:c.*343G>T	NP_001158888.1:n.*343G>T
NM_005566.3:c.*194G>T	NP_005557.1:n.*194G>T
NR_028500.1:n.1347G>T
NM_005566.4:c.*194G>T MANE Select	NP_005557.1:n.*194G>T
NM_001165415.2:c.*99G>T	NP_001158887.1:n.*99G>T
NM_001135239.2:c.*194G>T	NP_001128711.1:n.*194G>T
NM_001165414.2:c.*194G>T	NP_001158886.1:n.*194G>T
NM_001165416.2:c.*343G>T	NP_001158888.1:n.*343G>T
NR_028500.2:n.1173G>T