Canonical Allele Identifier: CA337722192

Gene: DDX3Y

Linked Data

• dbSNP Id: rs9341298
• gnomAD v3: Y-12911027-C-T
• gnomAD v4: Y-12911027-C-T
• MyVariant Identifiers: chrY:g.15022939C>T (hg19) ; chrY:g.12911027C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12911027C>T , CM000686.2:g.12911027C>T	GRCh38
NC_000024.9:g.15022939C>T , CM000686.1:g.15022939C>T	GRCh37
NC_000024.8:g.13532333C>T	NCBI36
NG_012831.1:g.11921C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.152-812C>T MANE Select	ENSP00000336725.3:n.152-812C>T
ENST00000336079.7:c.152-812C>T	ENSP00000336725.3:n.152-812C>T
ENST00000360160.8:c.152-812C>T	ENSP00000353284.4:n.152-812C>T
ENST00000440554.1:c.143-812C>T	ENSP00000400377.1:n.143-812C>T
ENST00000454054.5:c.152-812C>T	ENSP00000398953.1:n.152-812C>T
NM_001122665.2:c.152-812C>T	NP_001116137.1:n.152-812C>T
NM_001302552.1:c.143-812C>T	NP_001289481.1:n.143-812C>T
NM_004660.4:c.152-812C>T	NP_004651.2:n.152-812C>T
XM_006724878.1:c.152-812C>T	XP_006724941.1:n.152-812C>T
XM_011531471.1:c.152-812C>T	XP_011529773.1:n.152-812C>T
NM_001122665.3:c.152-812C>T	NP_001116137.1:n.152-812C>T
NM_001302552.2:c.143-812C>T	NP_001289481.1:n.143-812C>T
NM_001324195.1:c.152-812C>T	NP_001311124.1:n.152-812C>T
NR_136716.1:n.303-812C>T
NR_136717.1:n.303-812C>T
NR_136718.1:n.303-812C>T
NR_136719.1:n.302+1620C>T
NR_136720.1:n.303-812C>T
NR_136721.1:n.231-812C>T
NR_136722.1:n.218-812C>T
NR_136723.1:n.218-812C>T
NR_136724.1:n.218-812C>T
XR_001756014.2:n.256-812C>T
NM_004660.5:c.152-812C>T MANE Select	NP_004651.2:n.152-812C>T
NM_001302552.3:c.143-812C>T	NP_001289481.1:n.143-812C>T
NM_001324195.2:c.152-812C>T	NP_001311124.1:n.152-812C>T
NR_136716.2:n.221-812C>T
NR_136717.2:n.221-812C>T
NR_136718.2:n.221-812C>T
NR_136719.2:n.220+1620C>T
NR_136720.2:n.221-812C>T
NR_136721.2:n.221-812C>T