LDH info

Canonical Allele Identifier: CA11655294
Gene: SLC39A8 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10014145

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102279420A>G , CM000666.2:g.102279420A>G GRCh38
NC_000004.11:g.103200577A>G , CM000666.1:g.103200577A>G GRCh37
NC_000004.10:g.103419600A>G NCBI36
NG_047177.1:g.71079T>C

Transcript Alleles

HGVS Amino-acid change
NM_001135146.1:c.841-11341T>C VV NP_001128618.1:p.=
NM_001135147.1:c.841-11341T>C VV NP_001128619.1:p.=
NM_001135148.1:c.640-11341T>C VV NP_001128620.1:p.=
NM_022154.5:c.841-11341T>C VV NP_071437.3:p.=
XM_005263177.1:c.841-11341T>C XP_005263234.1:p.=
XM_011532182.1:c.199-11341T>C XP_011530484.1:p.=
XM_005263177.2:c.841-11341T>C XP_005263234.1:p.=
XM_017008541.1:c.640-11341T>C XP_016864030.1:p.=
XM_024454184.1:c.841-11341T>C XP_024309952.1:p.=
NM_001135146.2:c.841-11341T>C VV MANE Preferred NP_001128618.1:p.=
NM_001135148.2:c.640-11341T>C VV NP_001128620.1:p.=
ENST00000356736.4:c.841-11341T>C ENSP00000349174.4:p.=
ENST00000394833.6:c.841-11341T>C ENSP00000378310.2:p.=
ENST00000424970.6:c.841-11341T>C ENSP00000394548.2:p.=
ENST00000512337.1:n.173-9626T>C