Canonical Allele Identifier: CA519898521

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15026546T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914634T>A , CM000686.2:g.12914634T>A	GRCh38
NC_000024.9:g.15026546T>A , CM000686.1:g.15026546T>A	GRCh37
NC_000024.8:g.13535940T>A	NCBI36
NG_012831.1:g.15528T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.744T>A MANE Select	ENSP00000336725.3:p.Ala248=
ENST00000336079.7:c.744T>A	ENSP00000336725.3:p.Ala248=
ENST00000360160.8:c.744T>A	ENSP00000353284.4:p.Ala248=
ENST00000440554.1:c.735T>A	ENSP00000400377.1:p.Ala245=
ENST00000463199.1:n.262T>A
ENST00000472510.5:n.307T>A
NM_001122665.2:c.744T>A	NP_001116137.1:p.Ala248=
NM_001302552.1:c.735T>A	NP_001289481.1:p.Ala245=
NM_004660.4:c.744T>A	NP_004651.2:p.Ala248=
XM_006724878.1:c.744T>A	XP_006724941.1:p.Ala248=
XM_011531471.1:c.744T>A	XP_011529773.1:p.Ala248=
NM_001122665.3:c.744T>A	NP_001116137.1:p.Ala248=
NM_001302552.2:c.735T>A	NP_001289481.1:p.Ala245=
NM_001324195.1:c.744T>A	NP_001311124.1:p.Ala248=
NR_136716.1:n.895T>A
NR_136717.1:n.975T>A
NR_136718.1:n.975T>A
NR_136719.1:n.765T>A
NR_136720.1:n.895T>A
NR_136721.1:n.823T>A
NR_136722.1:n.890T>A
NR_136723.1:n.890T>A
NR_136724.1:n.810T>A
XR_001756014.2:n.848T>A
NM_004660.5:c.744T>A MANE Select	NP_004651.2:p.Ala248=
NM_001302552.3:c.735T>A	NP_001289481.1:p.Ala245=
NM_001324195.2:c.744T>A	NP_001311124.1:p.Ala248=
NR_136716.2:n.813T>A
NR_136717.2:n.893T>A
NR_136718.2:n.893T>A
NR_136719.2:n.683T>A
NR_136720.2:n.813T>A
NR_136721.2:n.813T>A