LDH info

Canonical Allele Identifier: CA7546848
Gene: SLC12A1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs774515747

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48226575A>T , CM000677.2:g.48226575A>T GRCh38
NC_000015.9:g.48518772A>T , CM000677.1:g.48518772A>T GRCh37
NC_000015.8:g.46306064A>T NCBI36
NG_021301.1:g.25275A>T

Transcript Alleles

HGVS Amino-acid change
NM_000338.2:c.724+4A>T VV NP_000329.2:p.=
NM_001184832.1:c.629-504A>T VV NP_001171761.1:p.=
XM_005254605.1:c.724+4A>T XP_005254662.1:p.=
XM_005254606.1:c.724+628A>T XP_005254663.1:p.=
XM_006720656.1:c.724+4A>T XP_006720719.1:p.=
XR_931896.1:n.940+4A>T
XM_005254606.2:c.724+628A>T XP_005254663.1:p.=
XR_001751524.2:n.363+886T>A
XR_001751525.1:n.363+886T>A
XR_002957762.1:n.363+886T>A
XR_932204.3:n.357+886T>A
NM_000338.3:c.724+4A>T VV MANE Preferred NP_000329.2:p.=
NM_001184832.2:c.629-504A>T VV NP_001171761.1:p.=
NM_001384136.1:c.724+628A>T VV NP_001371065.1:p.=
ENST00000330289.10:c.724+4A>T ENSP00000331550.6:p.=
ENST00000380993.7:c.724+4A>T ENSP00000370381.3:p.=
ENST00000396577.7:c.629-504A>T ENSP00000379822.3:p.=
ENST00000558252.5:n.4248A>T
ENST00000558405.5:c.724+4A>T ENSP00000453409.1:p.=
ENST00000559641.5:c.163+4A>T ENSP00000453230.1:p.=
ENST00000559723.2:n.97+628A>T
ENST00000560692.5:n.2250A>T
ENST00000561127.5:c.163+4A>T ENSP00000453602.2:p.=