Canonical Allele Identifier: CA5911526

Gene: LDHC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18412755T>C , CM000673.2:g.18412755T>C	GRCh38
NC_000011.9:g.18434302T>C , CM000673.1:g.18434302T>C	GRCh37
NC_000011.8:g.18390878T>C	NCBI36
NG_011816.1:g.5450T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541669.6:c.38T>C MANE Select	ENSP00000437783.1:p.Ile13Thr
ENST00000280704.8:c.38T>C	ENSP00000280704.3:p.Ile13Thr
ENST00000396215.7:c.38T>C	ENSP00000379518.3:p.Ile13Thr
ENST00000535809.1:c.38T>C	ENSP00000443997.1:p.Ile13Thr
ENST00000536880.5:c.38T>C	ENSP00000439555.1:p.Ile13Thr
ENST00000537486.5:c.38T>C	ENSP00000441478.1:p.Ile13Thr
ENST00000539369.1:c.38T>C	ENSP00000441991.1:p.Ile13Thr
ENST00000541669.5:c.38T>C	ENSP00000437783.1:p.Ile13Thr
ENST00000544105.5:c.38T>C	ENSP00000439060.1:p.Ile13Thr
ENST00000545848.5:c.38T>C	ENSP00000438196.1:p.Ile13Thr
ENST00000546146.5:c.38T>C	ENSP00000443414.1:p.Ile13Thr
NM_002301.4:c.38T>C	NP_002292.1:p.Ile13Thr
NM_017448.3:c.38T>C	NP_059144.1:p.Ile13Thr
XM_017017721.1:c.-193T>C	XP_016873210.1:n.-193T>C
XM_017017722.1:c.-193T>C	XP_016873211.1:n.-193T>C
NM_017448.4:c.38T>C	NP_059144.1:p.Ile13Thr
NM_017448.5:c.38T>C MANE Select	NP_059144.1:p.Ile13Thr
NM_002301.5:c.38T>C	NP_002292.1:p.Ile13Thr