Canonical Allele Identifier: CA2832053450
Gene: DDX3Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12908855dup , CM000686.2:g.12908855dup GRCh38
NC_000024.9:g.15020766dup , CM000686.1:g.15020766dup GRCh37
NC_000024.8:g.13530160dup NCBI36
NG_012831.1:g.9748dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.104-505dup MANE Select ENSP00000336725.3:n.104-505dup
ENST00000336079.7:c.104-505dup ENSP00000336725.3:n.104-505dup
ENST00000360160.8:c.104-505dup ENSP00000353284.4:n.104-505dup
ENST00000440554.1:c.95-505dup ENSP00000400377.1:n.95-505dup
ENST00000454054.5:c.104-505dup ENSP00000398953.1:n.104-505dup
ENST00000493363.1:n.192-505dup
NM_001122665.2:c.104-505dup NP_001116137.1:n.104-505dup
NM_001302552.1:c.95-505dup NP_001289481.1:n.95-505dup
NM_004660.4:c.104-505dup NP_004651.2:n.104-505dup
XM_006724878.1:c.104-505dup XP_006724941.1:n.104-505dup
XM_011531471.1:c.104-505dup XP_011529773.1:n.104-505dup
NM_001122665.3:c.104-505dup NP_001116137.1:n.104-505dup
NM_001302552.2:c.95-505dup NP_001289481.1:n.95-505dup
NM_001324195.1:c.104-505dup NP_001311124.1:n.104-505dup
NR_136716.1:n.255-505dup
NR_136717.1:n.255-505dup
NR_136718.1:n.255-505dup
NR_136719.1:n.255-505dup
NR_136720.1:n.255-505dup
NR_136721.1:n.183-505dup
NR_136722.1:n.170-505dup
NR_136723.1:n.170-505dup
NR_136724.1:n.170-505dup
XR_001756014.2:n.208-505dup
NM_004660.5:c.104-505dup MANE Select NP_004651.2:n.104-505dup
NM_001302552.3:c.95-505dup NP_001289481.1:n.95-505dup
NM_001324195.2:c.104-505dup NP_001311124.1:n.104-505dup
NR_136716.2:n.173-505dup
NR_136717.2:n.173-505dup
NR_136718.2:n.173-505dup
NR_136719.2:n.173-505dup
NR_136720.2:n.173-505dup
NR_136721.2:n.173-505dup