LDH info

Canonical Allele Identifier: CA5459611
Gene: MAP3K8 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1042058

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30439172T>C , CM000672.2:g.30439172T>C GRCh38
NC_000010.10:g.30728101T>C , CM000672.1:g.30728101T>C GRCh37
NC_000010.9:g.30768107T>C NCBI36
NG_029984.1:g.10152T>C

Transcript Alleles

HGVS Amino-acid change
NM_001244134.1:c.234T>C VV NP_001231063.1:p.Tyr78=
NM_005204.3:c.234T>C VV NP_005195.2:p.Tyr78=
XM_005252364.2:c.234T>C XP_005252421.2:p.Tyr78=
XM_011519308.1:c.549T>C XP_011517610.1:p.Tyr183=
XM_011519309.1:c.423+4424T>C XP_011517611.1:p.=
XM_011519310.1:c.234T>C XP_011517612.1:p.Tyr78=
XM_011519311.1:c.234T>C XP_011517613.1:p.Tyr78=
XM_011519312.1:c.234T>C XP_011517614.1:p.Tyr78=
XM_011519313.1:c.234T>C XP_011517615.1:p.Tyr78=
XM_011519314.1:c.234T>C XP_011517616.1:p.Tyr78=
XM_011519315.1:c.234T>C XP_011517617.1:p.Tyr78=
NM_001320961.1:c.234T>C VV NP_001307890.1:p.Tyr78=
XM_017015708.1:c.234T>C XP_016871197.1:p.Tyr78=
XM_017015709.2:c.234T>C XP_016871198.1:p.Tyr78=
XM_017015710.1:c.234T>C XP_016871199.1:p.Tyr78=
XM_017015711.2:c.-3618T>C XP_016871200.1:p.=
XM_017015712.1:c.-3618T>C XP_016871201.1:p.=
XM_017015713.1:c.-3618T>C XP_016871202.1:p.=
XM_017015714.1:c.-3618T>C XP_016871203.1:p.=
XM_024447819.1:c.-3618T>C XP_024303587.1:p.=
NM_005204.4:c.234T>C VV MANE Preferred NP_005195.2:p.Tyr78=
ENST00000263056.5:c.234T>C ENSP00000263056.1:p.Tyr78=
ENST00000375321.1:c.234T>C ENSP00000364470.1:p.Tyr78=
ENST00000375322.2:c.234T>C ENSP00000364471.1:p.Tyr78=
ENST00000413724.5:c.234T>C ENSP00000391275.1:p.Tyr78=
ENST00000415139.5:c.234T>C ENSP00000409653.1:p.Tyr78=
ENST00000542547.5:c.234T>C ENSP00000443610.1:p.Tyr78=