Canonical Allele Identifier: CA414992660

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15029397G>T (hg19) ; chrY:g.12917485G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917485G>T , CM000686.2:g.12917485G>T	GRCh38
NC_000024.9:g.15029397G>T , CM000686.1:g.15029397G>T	GRCh37
NC_000024.8:g.13538791G>T	NCBI36
NG_012831.1:g.18379G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1846G>T MANE Select	ENSP00000336725.3:p.Gly616Ter
ENST00000336079.7:c.1846G>T	ENSP00000336725.3:p.Gly616Ter
ENST00000360160.8:c.1846G>T	ENSP00000353284.4:p.Gly616Ter
NM_001122665.2:c.1846G>T	NP_001116137.1:p.Gly616Ter
NM_001302552.1:c.1837G>T	NP_001289481.1:p.Gly613Ter
NM_004660.4:c.1846G>T	NP_004651.2:p.Gly616Ter
XM_006724878.1:c.1777G>T	XP_006724941.1:p.Gly593Ter
NM_001122665.3:c.1846G>T	NP_001116137.1:p.Gly616Ter
NM_001302552.2:c.1837G>T	NP_001289481.1:p.Gly613Ter
NM_001324195.1:c.1777G>T	NP_001311124.1:p.Gly593Ter
NR_136716.1:n.2315G>T
NR_136717.1:n.2077G>T
NR_136718.1:n.2395G>T
NR_136719.1:n.2185G>T
NR_136720.1:n.2246G>T
NR_136721.1:n.1908G>T
NR_136722.1:n.1992G>T
NR_136723.1:n.2310G>T
NR_136724.1:n.2230G>T
XR_001756014.2:n.2010G>T
NM_004660.5:c.1846G>T MANE Select	NP_004651.2:p.Gly616Ter
NM_001302552.3:c.1837G>T	NP_001289481.1:p.Gly613Ter
NM_001324195.2:c.1777G>T	NP_001311124.1:p.Gly593Ter
NR_136716.2:n.2233G>T
NR_136717.2:n.1995G>T
NR_136718.2:n.2313G>T
NR_136719.2:n.2103G>T
NR_136720.2:n.2164G>T
NR_136721.2:n.1898G>T