Canonical Allele Identifier: CA414992653

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15029395G>C (hg19) ; chrY:g.12917483G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917483G>C , CM000686.2:g.12917483G>C	GRCh38
NC_000024.9:g.15029395G>C , CM000686.1:g.15029395G>C	GRCh37
NC_000024.8:g.13538789G>C	NCBI36
NG_012831.1:g.18377G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1844G>C MANE Select	ENSP00000336725.3:p.Arg615Pro
ENST00000336079.7:c.1844G>C	ENSP00000336725.3:p.Arg615Pro
ENST00000360160.8:c.1844G>C	ENSP00000353284.4:p.Arg615Pro
NM_001122665.2:c.1844G>C	NP_001116137.1:p.Arg615Pro
NM_001302552.1:c.1835G>C	NP_001289481.1:p.Arg612Pro
NM_004660.4:c.1844G>C	NP_004651.2:p.Arg615Pro
XM_006724878.1:c.1775G>C	XP_006724941.1:p.Arg592Pro
NM_001122665.3:c.1844G>C	NP_001116137.1:p.Arg615Pro
NM_001302552.2:c.1835G>C	NP_001289481.1:p.Arg612Pro
NM_001324195.1:c.1775G>C	NP_001311124.1:p.Arg592Pro
NR_136716.1:n.2313G>C
NR_136717.1:n.2075G>C
NR_136718.1:n.2393G>C
NR_136719.1:n.2183G>C
NR_136720.1:n.2244G>C
NR_136721.1:n.1906G>C
NR_136722.1:n.1990G>C
NR_136723.1:n.2308G>C
NR_136724.1:n.2228G>C
XR_001756014.2:n.2008G>C
NM_004660.5:c.1844G>C MANE Select	NP_004651.2:p.Arg615Pro
NM_001302552.3:c.1835G>C	NP_001289481.1:p.Arg612Pro
NM_001324195.2:c.1775G>C	NP_001311124.1:p.Arg592Pro
NR_136716.2:n.2231G>C
NR_136717.2:n.1993G>C
NR_136718.2:n.2311G>C
NR_136719.2:n.2101G>C
NR_136720.2:n.2162G>C
NR_136721.2:n.1896G>C