Canonical Allele Identifier: CA2612741994

Gene: LDHA

Linked Data

• gnomAD v4: 11-18407319-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407319C>T , CM000673.2:g.18407319C>T	GRCh38
NC_000011.9:g.18428866C>T , CM000673.1:g.18428866C>T	GRCh37
NC_000011.8:g.18385442C>T	NCBI36
NG_008185.1:g.17885C>T
NG_011816.1:g.14C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*38C>T MANE Select	ENSP00000395337.3:n.*38C>T
ENST00000227157.8:c.*187C>T	ENSP00000227157.4:n.*187C>T
ENST00000375710.7:n.1904C>T
ENST00000379412.9:c.*38C>T	ENSP00000368722.5:n.*38C>T
ENST00000396222.6:c.768C>T	ENSP00000379524.2:p.Tyr256=
ENST00000422447.7:c.*38C>T	ENSP00000395337.3:n.*38C>T
ENST00000430553.6:c.*38C>T	ENSP00000406172.2:n.*38C>T
ENST00000538451.1:n.924C>T
ENST00000540430.5:c.*38C>T	ENSP00000445175.1:n.*38C>T
ENST00000545215.5:c.*781C>T	ENSP00000442637.1:n.*781C>T
NM_001135239.1:c.*38C>T	NP_001128711.1:n.*38C>T
NM_001165414.1:c.*38C>T	NP_001158886.1:n.*38C>T
NM_001165415.1:c.768C>T	NP_001158887.1:p.Tyr256=
NM_001165416.1:c.*187C>T	NP_001158888.1:n.*187C>T
NM_005566.3:c.*38C>T	NP_005557.1:n.*38C>T
NR_028500.1:n.1191C>T
NM_005566.4:c.*38C>T MANE Select	NP_005557.1:n.*38C>T
NM_001165415.2:c.768C>T	NP_001158887.1:p.Tyr256=
NM_001135239.2:c.*38C>T	NP_001128711.1:n.*38C>T
NM_001165414.2:c.*38C>T	NP_001158886.1:n.*38C>T
NM_001165416.2:c.*187C>T	NP_001158888.1:n.*187C>T
NR_028500.2:n.1017C>T