Canonical Allele Identifier: CA5911467

Gene: LDHA

Linked Data

• dbSNP Id: rs138352370
• ExAC: 11:18428914 C / T
• gnomAD v2: 11-18428914-C-T
• gnomAD v3: 11-18407367-C-T
• gnomAD v4: 11-18407367-C-T
• MyVariant Identifiers: chr11:g.18428914C>T (hg19) ; chr11:g.18407367C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18407367C>T , CM000673.2:g.18407367C>T	GRCh38
NC_000011.9:g.18428914C>T , CM000673.1:g.18428914C>T	GRCh37
NC_000011.8:g.18385490C>T	NCBI36
NG_008185.1:g.17933C>T
NG_011816.1:g.62C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422447.8:c.*86C>T MANE Select	ENSP00000395337.3:n.*86C>T
ENST00000227157.8:c.*235C>T	ENSP00000227157.4:n.*235C>T
ENST00000375710.7:n.1952C>T
ENST00000379412.9:c.*86C>T	ENSP00000368722.5:n.*86C>T
ENST00000396222.6:c.816C>T	ENSP00000379524.2:p.Ile272=
ENST00000422447.7:c.*86C>T	ENSP00000395337.3:n.*86C>T
ENST00000430553.6:c.*86C>T	ENSP00000406172.2:n.*86C>T
ENST00000538451.1:n.972C>T
ENST00000540430.5:c.*86C>T	ENSP00000445175.1:n.*86C>T
ENST00000545215.5:c.*829C>T	ENSP00000442637.1:n.*829C>T
NM_001135239.1:c.*86C>T	NP_001128711.1:n.*86C>T
NM_001165414.1:c.*86C>T	NP_001158886.1:n.*86C>T
NM_001165415.1:c.816C>T	NP_001158887.1:p.Ile272=
NM_001165416.1:c.*235C>T	NP_001158888.1:n.*235C>T
NM_005566.3:c.*86C>T	NP_005557.1:n.*86C>T
NR_028500.1:n.1239C>T
NM_005566.4:c.*86C>T MANE Select	NP_005557.1:n.*86C>T
NM_001165415.2:c.816C>T	NP_001158887.1:p.Ile272=
NM_001135239.2:c.*86C>T	NP_001128711.1:n.*86C>T
NM_001165414.2:c.*86C>T	NP_001158886.1:n.*86C>T
NM_001165416.2:c.*235C>T	NP_001158888.1:n.*235C>T
NR_028500.2:n.1065C>T