Canonical Allele Identifier: CA473523875

Gene: LDHA

Linked Data

• gnomAD v4: 11-18407188-C-T
• MyVariant Identifiers: chr11:g.18428735C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407188C>T , CM000673.2:g.18407188C>T	GRCh38
NC_000011.9:g.18428735C>T , CM000673.1:g.18428735C>T	GRCh37
NC_000011.8:g.18385311C>T	NCBI36
NG_008185.1:g.17754C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.906C>T MANE Select	ENSP00000395337.3:p.Asp302=
ENST00000227157.8:c.*56C>T	ENSP00000227157.4:n.*56C>T
ENST00000375710.7:n.1773C>T
ENST00000379412.9:c.906C>T	ENSP00000368722.5:p.Asp302=
ENST00000396222.6:c.688-51C>T	ENSP00000379524.2:n.688-51C>T
ENST00000422447.7:c.906C>T	ENSP00000395337.3:p.Asp302=
ENST00000430553.6:c.732C>T	ENSP00000406172.2:p.Asp244=
ENST00000538451.1:n.793C>T
ENST00000540430.5:c.993C>T	ENSP00000445175.1:p.Asp331=
ENST00000542179.1:c.906C>T	ENSP00000445331.1:p.Asp302=
ENST00000545215.5:c.*650C>T	ENSP00000442637.1:n.*650C>T
NM_001135239.1:c.732C>T	NP_001128711.1:p.Asp244=
NM_001165414.1:c.993C>T	NP_001158886.1:p.Asp331=
NM_001165415.1:c.688-51C>T	NP_001158887.1:n.688-51C>T
NM_001165416.1:c.*56C>T	NP_001158888.1:n.*56C>T
NM_005566.3:c.906C>T	NP_005557.1:p.Asp302=
NR_028500.1:n.1060C>T
NM_005566.4:c.906C>T MANE Select	NP_005557.1:p.Asp302=
NM_001165415.2:c.688-51C>T	NP_001158887.1:n.688-51C>T
NM_001135239.2:c.732C>T	NP_001128711.1:p.Asp244=
NM_001165414.2:c.993C>T	NP_001158886.1:p.Asp331=
NM_001165416.2:c.*56C>T	NP_001158888.1:n.*56C>T
NR_028500.2:n.886C>T