LDH info

Canonical Allele Identifier: CA10712049
Gene: PRDM16 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2651899

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.3167148T>C , CM000663.2:g.3167148T>C GRCh38
NC_000001.10:g.3083712T>C , CM000663.1:g.3083712T>C GRCh37
NC_000001.9:g.3073572T>C NCBI36
NG_029576.1:g.102971T>C
NG_029576.2:g.102971T>C

Transcript Alleles

HGVS Amino-acid change
NM_022114.3:c.38-18977T>C VV NP_071397.3:p.=
NM_199454.2:c.38-18977T>C VV NP_955533.2:p.=
XM_005244772.3:c.38-18977T>C XP_005244829.1:p.=
XM_005244773.3:c.38-18977T>C XP_005244830.1:p.=
XM_005244774.3:c.38-18977T>C XP_005244831.1:p.=
XM_006710814.2:c.38-18977T>C XP_006710877.1:p.=
XM_011541944.1:c.38-18977T>C XP_011540246.1:p.=
XR_946881.1:n.426A>G
XR_946882.1:n.426A>G
XM_005244772.5:c.38-18977T>C XP_005244829.1:p.=
XM_005244773.5:c.38-18977T>C XP_005244830.1:p.=
XM_005244774.5:c.38-18977T>C XP_005244831.1:p.=
XM_006710814.4:c.38-18977T>C XP_006710877.1:p.=
XM_017002050.1:c.38-18977T>C XP_016857539.1:p.=
XR_001737867.1:n.450A>G
NM_022114.4:c.38-18977T>C VV MANE Preferred NP_071397.3:p.=
NM_199454.3:c.38-18977T>C VV NP_955533.2:p.=
ENST00000270722.9:c.38-18977T>C ENSP00000270722.5:p.=
ENST00000378391.6:c.38-18977T>C ENSP00000367643.2:p.=
ENST00000511072.5:c.38-18977T>C ENSP00000426975.1:p.=
ENST00000514189.5:c.38-18977T>C ENSP00000421400.1:p.=
ENST00000607632.1:n.115-18977T>C