LDH info

Canonical Allele Identifier: CA11873276
Gene: SLC2A9 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs6815001

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.9957038G>C , CM000666.2:g.9957038G>C GRCh38
NC_000004.11:g.9958662G>C , CM000666.1:g.9958662G>C GRCh37
NC_000004.10:g.9567760G>C NCBI36
NG_011540.1:g.88211C>G

Transcript Alleles

HGVS Amino-acid change
NM_001001290.1:c.595-14993C>G VV NP_001001290.1:p.=
NM_020041.2:c.682-14993C>G VV NP_064425.2:p.=
XM_006713968.2:c.682-14993C>G XP_006714031.1:p.=
XM_006713969.2:c.595-14993C>G XP_006714032.1:p.=
XM_011513856.1:c.682-14993C>G XP_011512158.1:p.=
XM_011513857.1:c.595-14993C>G XP_011512159.1:p.=
XM_011513858.1:c.595-14993C>G XP_011512160.1:p.=
XM_011513859.1:c.682-14993C>G XP_011512161.1:p.=
XM_011513860.1:c.682-14993C>G XP_011512162.1:p.=
XM_011513861.1:c.682-14993C>G XP_011512163.1:p.=
XM_011513862.1:c.286-14993C>G XP_011512164.1:p.=
XM_011513863.1:c.286-14993C>G XP_011512165.1:p.=
XM_011513864.1:c.274-14993C>G XP_011512166.1:p.=
XM_011513865.1:c.682-14993C>G XP_011512167.1:p.=
XM_011513866.1:c.682-14993C>G XP_011512168.1:p.=
XM_011513867.1:c.124-14993C>G XP_011512169.1:p.=
XM_011513868.1:c.682-14993C>G XP_011512170.1:p.=
XR_925341.1:n.778-14993C>G
XM_006713968.4:c.682-14993C>G XP_006714031.1:p.=
XM_011513856.3:c.682-14993C>G XP_011512158.1:p.=
XM_011513859.3:c.682-14993C>G XP_011512161.1:p.=
XM_011513860.3:c.682-14993C>G XP_011512162.1:p.=
XM_011513861.3:c.682-14993C>G XP_011512163.1:p.=
XM_011513862.3:c.286-14993C>G XP_011512164.1:p.=
XM_011513864.2:c.274-14993C>G XP_011512166.1:p.=
XM_011513865.2:c.682-14993C>G XP_011512167.1:p.=
XM_011513866.2:c.682-14993C>G XP_011512168.1:p.=
XM_011513867.3:c.124-14993C>G XP_011512169.1:p.=
XM_011513868.2:c.682-14993C>G XP_011512170.1:p.=
XM_017008457.2:c.682-14993C>G XP_016863946.1:p.=
XM_017008458.2:c.682-14993C>G XP_016863947.1:p.=
XM_017008459.1:c.220-14993C>G XP_016863948.1:p.=
XM_017008460.2:c.286-14993C>G XP_016863949.1:p.=
XM_024454150.1:c.682-14993C>G XP_024309918.1:p.=
XM_024454151.1:c.295-14993C>G XP_024309919.1:p.=
XM_024454152.1:c.682-14993C>G XP_024309920.1:p.=
XM_024454153.1:c.682-14993C>G XP_024309921.1:p.=
XR_001741290.1:n.855-14993C>G
XR_001741291.1:n.855-14993C>G
XR_925341.3:n.859-14993C>G
NM_020041.3:c.682-14993C>G VV MANE Preferred NP_064425.2:p.=
ENST00000264784.7:c.682-14993C>G ENSP00000264784.3:p.=
ENST00000309065.7:c.595-14993C>G ENSP00000311383.3:p.=
ENST00000505104.5:n.716-14993C>G
ENST00000506583.5:c.595-14993C>G ENSP00000422209.1:p.=