Canonical Allele Identifier: CA414992698

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15029404G>C (hg19) ; chrY:g.12917492G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917492G>C , CM000686.2:g.12917492G>C	GRCh38
NC_000024.9:g.15029404G>C , CM000686.1:g.15029404G>C	GRCh37
NC_000024.8:g.13538798G>C	NCBI36
NG_012831.1:g.18386G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1853G>C MANE Select	ENSP00000336725.3:p.Ser618Thr
ENST00000336079.7:c.1853G>C	ENSP00000336725.3:p.Ser618Thr
ENST00000360160.8:c.1853G>C	ENSP00000353284.4:p.Ser618Thr
NM_001122665.2:c.1853G>C	NP_001116137.1:p.Ser618Thr
NM_001302552.1:c.1844G>C	NP_001289481.1:p.Ser615Thr
NM_004660.4:c.1853G>C	NP_004651.2:p.Ser618Thr
XM_006724878.1:c.1784G>C	XP_006724941.1:p.Ser595Thr
NM_001122665.3:c.1853G>C	NP_001116137.1:p.Ser618Thr
NM_001302552.2:c.1844G>C	NP_001289481.1:p.Ser615Thr
NM_001324195.1:c.1784G>C	NP_001311124.1:p.Ser595Thr
NR_136716.1:n.2322G>C
NR_136717.1:n.2084G>C
NR_136718.1:n.2402G>C
NR_136719.1:n.2192G>C
NR_136720.1:n.2253G>C
NR_136721.1:n.1915G>C
NR_136722.1:n.1999G>C
NR_136723.1:n.2317G>C
NR_136724.1:n.2237G>C
XR_001756014.2:n.2017G>C
NM_004660.5:c.1853G>C MANE Select	NP_004651.2:p.Ser618Thr
NM_001302552.3:c.1844G>C	NP_001289481.1:p.Ser615Thr
NM_001324195.2:c.1784G>C	NP_001311124.1:p.Ser595Thr
NR_136716.2:n.2240G>C
NR_136717.2:n.2002G>C
NR_136718.2:n.2320G>C
NR_136719.2:n.2110G>C
NR_136720.2:n.2171G>C
NR_136721.2:n.1905G>C