Canonical Allele Identifier: CA337722209
Gene: DDX3Y HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12911452T>C , CM000686.2:g.12911452T>C GRCh38
NC_000024.9:g.15023364T>C , CM000686.1:g.15023364T>C GRCh37
NC_000024.8:g.13532758T>C NCBI36
NG_012831.1:g.12346T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.152-387T>C MANE Select ENSP00000336725.3:n.152-387T>C
ENST00000336079.7:c.152-387T>C ENSP00000336725.3:n.152-387T>C
ENST00000360160.8:c.152-387T>C ENSP00000353284.4:n.152-387T>C
ENST00000440554.1:c.143-387T>C ENSP00000400377.1:n.143-387T>C
ENST00000454054.5:c.152-387T>C ENSP00000398953.1:n.152-387T>C
NM_001122665.2:c.152-387T>C NP_001116137.1:n.152-387T>C
NM_001302552.1:c.143-387T>C NP_001289481.1:n.143-387T>C
NM_004660.4:c.152-387T>C NP_004651.2:n.152-387T>C
XM_006724878.1:c.152-387T>C XP_006724941.1:n.152-387T>C
XM_011531471.1:c.152-387T>C XP_011529773.1:n.152-387T>C
NM_001122665.3:c.152-387T>C NP_001116137.1:n.152-387T>C
NM_001302552.2:c.143-387T>C NP_001289481.1:n.143-387T>C
NM_001324195.1:c.152-387T>C NP_001311124.1:n.152-387T>C
NR_136716.1:n.303-387T>C
NR_136717.1:n.303-387T>C
NR_136718.1:n.303-387T>C
NR_136719.1:n.303-1275T>C
NR_136720.1:n.303-387T>C
NR_136721.1:n.231-387T>C
NR_136722.1:n.218-387T>C
NR_136723.1:n.218-387T>C
NR_136724.1:n.218-387T>C
XR_001756014.2:n.256-387T>C
NM_004660.5:c.152-387T>C MANE Select NP_004651.2:n.152-387T>C
NM_001302552.3:c.143-387T>C NP_001289481.1:n.143-387T>C
NM_001324195.2:c.152-387T>C NP_001311124.1:n.152-387T>C
NR_136716.2:n.221-387T>C
NR_136717.2:n.221-387T>C
NR_136718.2:n.221-387T>C
NR_136719.2:n.221-1275T>C
NR_136720.2:n.221-387T>C
NR_136721.2:n.221-387T>C
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