Canonical Allele Identifier: CA414992666

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15029398G>C (hg19) ; chrY:g.12917486G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917486G>C , CM000686.2:g.12917486G>C	GRCh38
NC_000024.9:g.15029398G>C , CM000686.1:g.15029398G>C	GRCh37
NC_000024.8:g.13538792G>C	NCBI36
NG_012831.1:g.18380G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1847G>C MANE Select	ENSP00000336725.3:p.Gly616Ala
ENST00000336079.7:c.1847G>C	ENSP00000336725.3:p.Gly616Ala
ENST00000360160.8:c.1847G>C	ENSP00000353284.4:p.Gly616Ala
NM_001122665.2:c.1847G>C	NP_001116137.1:p.Gly616Ala
NM_001302552.1:c.1838G>C	NP_001289481.1:p.Gly613Ala
NM_004660.4:c.1847G>C	NP_004651.2:p.Gly616Ala
XM_006724878.1:c.1778G>C	XP_006724941.1:p.Gly593Ala
NM_001122665.3:c.1847G>C	NP_001116137.1:p.Gly616Ala
NM_001302552.2:c.1838G>C	NP_001289481.1:p.Gly613Ala
NM_001324195.1:c.1778G>C	NP_001311124.1:p.Gly593Ala
NR_136716.1:n.2316G>C
NR_136717.1:n.2078G>C
NR_136718.1:n.2396G>C
NR_136719.1:n.2186G>C
NR_136720.1:n.2247G>C
NR_136721.1:n.1909G>C
NR_136722.1:n.1993G>C
NR_136723.1:n.2311G>C
NR_136724.1:n.2231G>C
XR_001756014.2:n.2011G>C
NM_004660.5:c.1847G>C MANE Select	NP_004651.2:p.Gly616Ala
NM_001302552.3:c.1838G>C	NP_001289481.1:p.Gly613Ala
NM_001324195.2:c.1778G>C	NP_001311124.1:p.Gly593Ala
NR_136716.2:n.2234G>C
NR_136717.2:n.1996G>C
NR_136718.2:n.2314G>C
NR_136719.2:n.2104G>C
NR_136720.2:n.2165G>C
NR_136721.2:n.1899G>C