Canonical Allele Identifier: CA414983493

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15025669A>T (hg19) ; chrY:g.12913757A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12913757A>T , CM000686.2:g.12913757A>T	GRCh38
NC_000024.9:g.15025669A>T , CM000686.1:g.15025669A>T	GRCh37
NC_000024.8:g.13535063A>T	NCBI36
NG_012831.1:g.14651A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.577A>T MANE Select	ENSP00000336725.3:p.Ile193Phe
ENST00000336079.7:c.577A>T	ENSP00000336725.3:p.Ile193Phe
ENST00000360160.8:c.577A>T	ENSP00000353284.4:p.Ile193Phe
ENST00000440554.1:c.568A>T	ENSP00000400377.1:p.Ile190Phe
ENST00000454054.5:c.577A>T	ENSP00000398953.1:p.Ile193Phe
ENST00000463199.1:n.95A>T
ENST00000469101.1:n.463A>T
ENST00000472510.5:n.140A>T
NM_001122665.2:c.577A>T	NP_001116137.1:p.Ile193Phe
NM_001302552.1:c.568A>T	NP_001289481.1:p.Ile190Phe
NM_004660.4:c.577A>T	NP_004651.2:p.Ile193Phe
XM_006724878.1:c.577A>T	XP_006724941.1:p.Ile193Phe
XM_011531471.1:c.577A>T	XP_011529773.1:p.Ile193Phe
NM_001122665.3:c.577A>T	NP_001116137.1:p.Ile193Phe
NM_001302552.2:c.568A>T	NP_001289481.1:p.Ile190Phe
NM_001324195.1:c.577A>T	NP_001311124.1:p.Ile193Phe
NR_136716.1:n.728A>T
NR_136717.1:n.808A>T
NR_136718.1:n.808A>T
NR_136719.1:n.598A>T
NR_136720.1:n.728A>T
NR_136721.1:n.656A>T
NR_136722.1:n.723A>T
NR_136723.1:n.723A>T
NR_136724.1:n.643A>T
XR_001756014.2:n.681A>T
NM_004660.5:c.577A>T MANE Select	NP_004651.2:p.Ile193Phe
NM_001302552.3:c.568A>T	NP_001289481.1:p.Ile190Phe
NM_001324195.2:c.577A>T	NP_001311124.1:p.Ile193Phe
NR_136716.2:n.646A>T
NR_136717.2:n.726A>T
NR_136718.2:n.726A>T
NR_136719.2:n.516A>T
NR_136720.2:n.646A>T
NR_136721.2:n.646A>T