Canonical Allele Identifier: CA414992761

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15029412A>T (hg19) ; chrY:g.12917500A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917500A>T , CM000686.2:g.12917500A>T	GRCh38
NC_000024.9:g.15029412A>T , CM000686.1:g.15029412A>T	GRCh37
NC_000024.8:g.13538806A>T	NCBI36
NG_012831.1:g.18394A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1861A>T MANE Select	ENSP00000336725.3:p.Ser621Cys
ENST00000336079.7:c.1861A>T	ENSP00000336725.3:p.Ser621Cys
ENST00000360160.8:c.1861A>T	ENSP00000353284.4:p.Ser621Cys
NM_001122665.2:c.1861A>T	NP_001116137.1:p.Ser621Cys
NM_001302552.1:c.1852A>T	NP_001289481.1:p.Ser618Cys
NM_004660.4:c.1861A>T	NP_004651.2:p.Ser621Cys
XM_006724878.1:c.1792A>T	XP_006724941.1:p.Ser598Cys
NM_001122665.3:c.1861A>T	NP_001116137.1:p.Ser621Cys
NM_001302552.2:c.1852A>T	NP_001289481.1:p.Ser618Cys
NM_001324195.1:c.1792A>T	NP_001311124.1:p.Ser598Cys
NR_136716.1:n.2330A>T
NR_136717.1:n.2092A>T
NR_136718.1:n.2410A>T
NR_136719.1:n.2200A>T
NR_136720.1:n.2261A>T
NR_136721.1:n.1923A>T
NR_136722.1:n.2007A>T
NR_136723.1:n.2325A>T
NR_136724.1:n.2245A>T
XR_001756014.2:n.2025A>T
NM_004660.5:c.1861A>T MANE Select	NP_004651.2:p.Ser621Cys
NM_001302552.3:c.1852A>T	NP_001289481.1:p.Ser618Cys
NM_001324195.2:c.1792A>T	NP_001311124.1:p.Ser598Cys
NR_136716.2:n.2248A>T
NR_136717.2:n.2010A>T
NR_136718.2:n.2328A>T
NR_136719.2:n.2118A>T
NR_136720.2:n.2179A>T
NR_136721.2:n.1913A>T