Canonical Allele Identifier: CA5911517

Gene: LDHC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18412724A>G , CM000673.2:g.18412724A>G	GRCh38
NC_000011.9:g.18434271A>G , CM000673.1:g.18434271A>G	GRCh37
NC_000011.8:g.18390847A>G	NCBI36
NG_011816.1:g.5419A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541669.6:c.7A>G MANE Select	ENSP00000437783.1:p.Thr3Ala
ENST00000280704.8:c.7A>G	ENSP00000280704.3:p.Thr3Ala
ENST00000396215.7:c.7A>G	ENSP00000379518.3:p.Thr3Ala
ENST00000535809.1:c.7A>G	ENSP00000443997.1:p.Thr3Ala
ENST00000536880.5:c.7A>G	ENSP00000439555.1:p.Thr3Ala
ENST00000537486.5:c.7A>G	ENSP00000441478.1:p.Thr3Ala
ENST00000539369.1:c.7A>G	ENSP00000441991.1:p.Thr3Ala
ENST00000541669.5:c.7A>G	ENSP00000437783.1:p.Thr3Ala
ENST00000544105.5:c.7A>G	ENSP00000439060.1:p.Thr3Ala
ENST00000545848.5:c.7A>G	ENSP00000438196.1:p.Thr3Ala
ENST00000546146.5:c.7A>G	ENSP00000443414.1:p.Thr3Ala
NM_002301.4:c.7A>G	NP_002292.1:p.Thr3Ala
NM_017448.3:c.7A>G	NP_059144.1:p.Thr3Ala
XM_017017721.1:c.-224A>G	XP_016873210.1:n.-224A>G
XM_017017722.1:c.-224A>G	XP_016873211.1:n.-224A>G
NM_017448.4:c.7A>G	NP_059144.1:p.Thr3Ala
NM_017448.5:c.7A>G MANE Select	NP_059144.1:p.Thr3Ala
NM_002301.5:c.7A>G	NP_002292.1:p.Thr3Ala