LDH info

Canonical Allele Identifier: CA5987182
Gene: FOLH1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs202676

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.49206068A>G , CM000673.2:g.49206068A>G GRCh38
NC_000011.9:g.49227620A>G , CM000673.1:g.49227620A>G GRCh37
NC_000011.8:g.49184196A>G NCBI36
NG_029170.1:g.7603T>C

Transcript Alleles

HGVS Amino-acid change
NM_001014986.1:c.223T>C VV NP_001014986.1:p.Tyr75His
NM_001193471.1:c.178T>C VV NP_001180400.1:p.Tyr60His
NM_001193472.1:c.178T>C VV NP_001180401.1:p.Tyr60His
NM_001193473.1:c.-328T>C VV NP_001180402.1:p.=
NM_004476.1:c.223T>C VV NP_004467.1:p.Tyr75His
XM_011519958.1:c.178T>C XP_011518260.1:p.Tyr60His
NM_001014986.2:c.223T>C VV NP_001014986.1:p.Tyr75His
NM_001193471.2:c.178T>C VV NP_001180400.1:p.Tyr60His
NM_001193472.2:c.178T>C VV NP_001180401.1:p.Tyr60His
NM_001193473.2:c.-328T>C VV NP_001180402.1:p.=
NM_001351236.1:c.52T>C VV NP_001338165.1:p.Tyr18His
NM_004476.2:c.223T>C VV NP_004467.1:p.Tyr75His
XM_011519958.3:c.388T>C XP_011518260.2:p.Tyr130His
XM_017017432.1:c.388T>C XP_016872921.1:p.Tyr130His
XM_017017433.2:c.388T>C XP_016872922.1:p.Tyr130His
XM_017017434.1:c.178T>C XP_016872923.1:p.Tyr60His
XM_017017435.2:c.178T>C XP_016872924.1:p.Tyr60His
XM_017017444.2:c.-515T>C XP_016872933.1:p.=
XM_017017445.1:c.-515T>C XP_016872934.1:p.=
XM_017017446.1:c.-515T>C XP_016872935.1:p.=
XM_017017447.1:c.-515T>C XP_016872936.1:p.=
XM_017017448.1:c.-515T>C XP_016872937.1:p.=
XM_017017449.2:c.-515T>C XP_016872938.1:p.=
XM_017017450.2:c.-515T>C XP_016872939.1:p.=
XM_017017451.2:c.-515T>C XP_016872940.1:p.=
XM_024448411.1:c.-3916T>C XP_024304179.1:p.=
XR_001747818.1:n.618T>C
XR_001747819.1:n.450T>C
NM_004476.3:c.223T>C VV MANE Preferred NP_004467.1:p.Tyr75His
NM_001014986.3:c.223T>C VV NP_001014986.1:p.Tyr75His
NM_001193471.3:c.178T>C VV NP_001180400.1:p.Tyr60His
NM_001193472.3:c.178T>C VV NP_001180401.1:p.Tyr60His
NM_001193473.3:c.-328T>C VV NP_001180402.1:p.=
NM_001351236.2:c.52T>C VV NP_001338165.1:p.Tyr18His
ENST00000256999.6:c.223T>C ENSP00000256999.2:p.Tyr75His
ENST00000340334.11:c.178T>C ENSP00000344131.7:p.Tyr60His
ENST00000343844.8:c.-328T>C ENSP00000344086.4:p.=
ENST00000356696.7:c.223T>C ENSP00000349129.3:p.Tyr75His
ENST00000525826.5:c.223T>C ENSP00000434928.1:p.Ter75Gln
ENST00000529117.1:c.52T>C ENSP00000431577.1:p.Tyr18His
ENST00000529646.5:n.238T>C
ENST00000529648.1:c.*214T>C ENSP00000431263.1:p.=
ENST00000533034.1:c.178T>C ENSP00000431463.1:p.Tyr60His
ENST00000533510.5:c.*135T>C ENSP00000436569.1:p.=