LDH info

Canonical Allele Identifier: CA11968648
Gene: ARL15 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4311394

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.54004832A>G , CM000667.2:g.54004832A>G GRCh38
NC_000005.9:g.53300662A>G , CM000667.1:g.53300662A>G GRCh37
NC_000005.8:g.53336419A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_019087.2:c.462+108370T>C VV NP_061960.1:p.=
XM_011543498.1:c.645+108370T>C XP_011541800.1:p.=
XM_011543499.1:c.588+108370T>C XP_011541801.1:p.=
XM_011543500.1:c.519+108370T>C XP_011541802.1:p.=
XM_011543498.2:c.645+108370T>C XP_011541800.1:p.=
XM_011543499.2:c.588+108370T>C XP_011541801.1:p.=
XM_011543500.2:c.519+108370T>C XP_011541802.1:p.=
XM_017009598.1:c.468+108370T>C XP_016865087.1:p.=
NM_019087.3:c.462+108370T>C VV MANE Preferred NP_061960.1:p.=
ENST00000502271.5:c.-76+108370T>C ENSP00000473508.1:p.=
ENST00000504924.5:c.462+108370T>C ENSP00000433427.1:p.=
ENST00000507646.2:c.462+108370T>C ENSP00000432680.1:p.=
ENST00000510591.6:n.535+108370T>C
ENST00000620747.4:c.468+62330T>C ENSP00000478984.1:p.=