Canonical Allele Identifier: CA1139170999

Gene: DDX3Y

Linked Data

• gnomAD v3: Y-12917585-T-C
• gnomAD v4: Y-12917585-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917585T>C , CM000686.2:g.12917585T>C	GRCh38
NC_000024.9:g.15029497T>C , CM000686.1:g.15029497T>C	GRCh37
NC_000024.8:g.13538891T>C	NCBI36
NG_012831.1:g.18479T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1903+43T>C MANE Select	ENSP00000336725.3:n.1903+43T>C
ENST00000336079.7:c.1903+43T>C	ENSP00000336725.3:n.1903+43T>C
ENST00000360160.8:c.1903+43T>C	ENSP00000353284.4:n.1903+43T>C
NM_001122665.2:c.1903+43T>C	NP_001116137.1:n.1903+43T>C
NM_001302552.1:c.1894+43T>C	NP_001289481.1:n.1894+43T>C
NM_004660.4:c.1903+43T>C	NP_004651.2:n.1903+43T>C
XM_006724878.1:c.1834+43T>C	XP_006724941.1:n.1834+43T>C
NM_001122665.3:c.1903+43T>C	NP_001116137.1:n.1903+43T>C
NM_001302552.2:c.1894+43T>C	NP_001289481.1:n.1894+43T>C
NM_001324195.1:c.1834+43T>C	NP_001311124.1:n.1834+43T>C
NR_136716.1:n.2372+43T>C
NR_136717.1:n.2134+43T>C
NR_136718.1:n.2452+43T>C
NR_136719.1:n.2242+43T>C
NR_136720.1:n.2303+43T>C
NR_136721.1:n.1965+43T>C
NR_136722.1:n.2049+43T>C
NR_136723.1:n.2367+43T>C
NR_136724.1:n.2287+43T>C
XR_001756014.2:n.2067+43T>C
NM_004660.5:c.1903+43T>C MANE Select	NP_004651.2:n.1903+43T>C
NM_001302552.3:c.1894+43T>C	NP_001289481.1:n.1894+43T>C
NM_001324195.2:c.1834+43T>C	NP_001311124.1:n.1834+43T>C
NR_136716.2:n.2290+43T>C
NR_136717.2:n.2052+43T>C
NR_136718.2:n.2370+43T>C
NR_136719.2:n.2160+43T>C
NR_136720.2:n.2221+43T>C
NR_136721.2:n.1955+43T>C