Canonical Allele Identifier: CA473523866

Gene: LDHA

Linked Data

• MyVariant Identifiers: chr11:g.18428723T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407176T>C , CM000673.2:g.18407176T>C	GRCh38
NC_000011.9:g.18428723T>C , CM000673.1:g.18428723T>C	GRCh37
NC_000011.8:g.18385299T>C	NCBI36
NG_008185.1:g.17742T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000422447.8:c.894T>C MANE Select	ENSP00000395337.3:p.Asn298=
ENST00000227157.8:c.*44T>C	ENSP00000227157.4:n.*44T>C
ENST00000375710.7:n.1761T>C
ENST00000379412.9:c.894T>C	ENSP00000368722.5:p.Asn298=
ENST00000396222.6:c.688-63T>C	ENSP00000379524.2:n.688-63T>C
ENST00000422447.7:c.894T>C	ENSP00000395337.3:p.Asn298=
ENST00000430553.6:c.720T>C	ENSP00000406172.2:p.Asn240=
ENST00000538451.1:n.781T>C
ENST00000540430.5:c.981T>C	ENSP00000445175.1:p.Asn327=
ENST00000542179.1:c.894T>C	ENSP00000445331.1:p.Asn298=
ENST00000545215.5:c.*638T>C	ENSP00000442637.1:n.*638T>C
NM_001135239.1:c.720T>C	NP_001128711.1:p.Asn240=
NM_001165414.1:c.981T>C	NP_001158886.1:p.Asn327=
NM_001165415.1:c.688-63T>C	NP_001158887.1:n.688-63T>C
NM_001165416.1:c.*44T>C	NP_001158888.1:n.*44T>C
NM_005566.3:c.894T>C	NP_005557.1:p.Asn298=
NR_028500.1:n.1048T>C
NM_005566.4:c.894T>C MANE Select	NP_005557.1:p.Asn298=
NM_001165415.2:c.688-63T>C	NP_001158887.1:n.688-63T>C
NM_001135239.2:c.720T>C	NP_001128711.1:p.Asn240=
NM_001165414.2:c.981T>C	NP_001158886.1:p.Asn327=
NM_001165416.2:c.*44T>C	NP_001158888.1:n.*44T>C
NR_028500.2:n.874T>C