Canonical Allele Identifier: CA2612742077

Gene: LDHA

Linked Data

• gnomAD v4: 11-18407464-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407464T>C , CM000673.2:g.18407464T>C	GRCh38
NC_000011.9:g.18429011T>C , CM000673.1:g.18429011T>C	GRCh37
NC_000011.8:g.18385587T>C	NCBI36
NG_008185.1:g.18030T>C
NG_011816.1:g.159T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*183T>C MANE Select	ENSP00000395337.3:n.*183T>C
ENST00000227157.8:c.*332T>C	ENSP00000227157.4:n.*332T>C
ENST00000375710.7:n.2049T>C
ENST00000379412.9:c.*183T>C	ENSP00000368722.5:n.*183T>C
ENST00000396222.6:c.*88T>C	ENSP00000379524.2:n.*88T>C
ENST00000422447.7:c.*183T>C	ENSP00000395337.3:n.*183T>C
ENST00000430553.6:c.*183T>C	ENSP00000406172.2:n.*183T>C
ENST00000538451.1:n.1069T>C
ENST00000540430.5:c.*183T>C	ENSP00000445175.1:n.*183T>C
ENST00000545215.5:c.*926T>C	ENSP00000442637.1:n.*926T>C
NM_001135239.1:c.*183T>C	NP_001128711.1:n.*183T>C
NM_001165414.1:c.*183T>C	NP_001158886.1:n.*183T>C
NM_001165415.1:c.*88T>C	NP_001158887.1:n.*88T>C
NM_001165416.1:c.*332T>C	NP_001158888.1:n.*332T>C
NM_005566.3:c.*183T>C	NP_005557.1:n.*183T>C
NR_028500.1:n.1336T>C
NM_005566.4:c.*183T>C MANE Select	NP_005557.1:n.*183T>C
NM_001165415.2:c.*88T>C	NP_001158887.1:n.*88T>C
NM_001135239.2:c.*183T>C	NP_001128711.1:n.*183T>C
NM_001165414.2:c.*183T>C	NP_001158886.1:n.*183T>C
NM_001165416.2:c.*332T>C	NP_001158888.1:n.*332T>C
NR_028500.2:n.1162T>C