LDH info

Canonical Allele Identifier: CA15856860
Gene: ADAM10 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs347117

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58708758C>T , CM000677.2:g.58708758C>T GRCh38
NC_000015.9:g.59000957C>T , CM000677.1:g.59000957C>T GRCh37
NC_000015.8:g.56788249C>T NCBI36
NG_033876.1:g.46221G>A
NG_033876.2:g.45950G>A

Transcript Alleles

HGVS Amino-acid change
NM_001110.3:c.206+8819G>A VV NP_001101.1:p.=
XM_005254117.2:c.206+8819G>A XP_005254174.1:p.=
NM_001320570.1:c.206+8819G>A VV NP_001307499.1:p.=
XM_024449818.1:c.-17+8819G>A XP_024305586.1:p.=
NM_001110.4:c.206+8819G>A VV MANE Preferred NP_001101.1:p.=
NM_001320570.2:c.206+8819G>A VV NP_001307499.1:p.=
ENST00000260408.7:c.206+8819G>A ENSP00000260408.3:p.=
ENST00000402627.5:c.55+40722G>A ENSP00000386056.1:p.=
ENST00000439637.5:c.206+8819G>A ENSP00000391930.1:p.=
ENST00000497846.5:n.323+8819G>A
ENST00000558004.1:c.206+8819G>A ENSP00000452704.1:p.=
ENST00000558733.5:n.442+8819G>A
ENST00000559053.1:c.55+40722G>A ENSP00000453952.1:p.=
ENST00000560608.5:n.463+8819G>A
ENST00000561149.1:n.393-1378G>A
ENST00000561288.1:c.55+40722G>A ENSP00000452639.1:p.=