LDH info

Canonical Allele Identifier: CA337722284
Gene: DDX3Y HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2032636
MyVariant Identifiers: chrY:g.12915617G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12915617G>T , CM000686.2:g.12915617G>T GRCh38

Transcript Alleles

HGVS Amino-acid change
NM_001122665.2:c.1020-13G>T VV NP_001116137.1:p.=
NM_001302552.1:c.1011-13G>T VV NP_001289481.1:p.=
NM_004660.4:c.1020-13G>T VV NP_004651.2:p.=
XM_006724878.1:c.1020-13G>T XP_006724941.1:p.=
XM_011531471.1:c.1020-13G>T XP_011529773.1:p.=
NM_001122665.3:c.1020-13G>T VV NP_001116137.1:p.=
NM_001302552.2:c.1011-13G>T VV NP_001289481.1:p.=
NM_001324195.1:c.1020-13G>T VV NP_001311124.1:p.=
NR_136716.1:n.1489-13G>T
NR_136717.1:n.1251-13G>T
NR_136718.1:n.1569-13G>T
NR_136719.1:n.1359-13G>T
NR_136720.1:n.1489-13G>T
NR_136721.1:n.1082-13G>T
NR_136722.1:n.1166-13G>T
NR_136723.1:n.1484-13G>T
NR_136724.1:n.1404-13G>T
XR_001756014.2:n.1124-13G>T
NM_004660.5:c.1020-13G>T VV MANE Preferred NP_004651.2:p.=
NM_001302552.3:c.1011-13G>T VV NP_001289481.1:p.=
NM_001324195.2:c.1020-13G>T VV NP_001311124.1:p.=
NR_136716.2:n.1407-13G>T
NR_136717.2:n.1169-13G>T
NR_136718.2:n.1487-13G>T
NR_136719.2:n.1277-13G>T
NR_136720.2:n.1407-13G>T
NR_136721.2:n.1072-13G>T
ENST00000336079.7:c.1020-13G>T ENSP00000336725.3:p.=
ENST00000360160.8:c.1020-13G>T ENSP00000353284.4:p.=
ENST00000495478.1:n.122G>T