Canonical Allele Identifier: CA379508702

Gene: LDHA

Linked Data

• MyVariant Identifiers: chr11:g.18428689T>C (hg19) ; chr11:g.18407142T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407142T>C , CM000673.2:g.18407142T>C	GRCh38
NC_000011.9:g.18428689T>C , CM000673.1:g.18428689T>C	GRCh37
NC_000011.8:g.18385265T>C	NCBI36
NG_008185.1:g.17708T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.860T>C MANE Select	ENSP00000395337.3:p.Val287Ala
ENST00000227157.8:c.*10T>C	ENSP00000227157.4:n.*10T>C
ENST00000375710.7:n.1727T>C
ENST00000379412.9:c.860T>C	ENSP00000368722.5:p.Val287Ala
ENST00000396222.6:c.688-97T>C	ENSP00000379524.2:n.688-97T>C
ENST00000422447.7:c.860T>C	ENSP00000395337.3:p.Val287Ala
ENST00000430553.6:c.686T>C	ENSP00000406172.2:p.Val229Ala
ENST00000538451.1:n.747T>C
ENST00000540430.5:c.947T>C	ENSP00000445175.1:p.Val316Ala
ENST00000541097.5:c.*198T>C	ENSP00000443362.1:n.*198T>C
ENST00000542179.1:c.860T>C	ENSP00000445331.1:p.Val287Ala
ENST00000545215.5:c.*604T>C	ENSP00000442637.1:n.*604T>C
NM_001135239.1:c.686T>C	NP_001128711.1:p.Val229Ala
NM_001165414.1:c.947T>C	NP_001158886.1:p.Val316Ala
NM_001165415.1:c.688-97T>C	NP_001158887.1:n.688-97T>C
NM_001165416.1:c.*10T>C	NP_001158888.1:n.*10T>C
NM_005566.3:c.860T>C	NP_005557.1:p.Val287Ala
NR_028500.1:n.1014T>C
NM_005566.4:c.860T>C MANE Select	NP_005557.1:p.Val287Ala
NM_001165415.2:c.688-97T>C	NP_001158887.1:n.688-97T>C
NM_001135239.2:c.686T>C	NP_001128711.1:p.Val229Ala
NM_001165414.2:c.947T>C	NP_001158886.1:p.Val316Ala
NM_001165416.2:c.*10T>C	NP_001158888.1:n.*10T>C
NR_028500.2:n.840T>C