Canonical Allele Identifier: CA2540369194

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917601_12917602insTTT , CM000686.2:g.12917601_12917602insTTT	GRCh38
NC_000024.9:g.15029513_15029514insTTT , CM000686.1:g.15029513_15029514insTTT	GRCh37
NC_000024.8:g.13538907_13538908insTTT	NCBI36
NG_012831.1:g.18495_18496insTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1903+59_1903+60insTTT MANE Select	ENSP00000336725.3:n.1903+59_1903+60insTTT...
ENST00000336079.7:c.1903+59_1903+60insTTT	ENSP00000336725.3:n.1903+59_1903+60insTTT...
ENST00000360160.8:c.1903+59_1903+60insTTT	ENSP00000353284.4:n.1903+59_1903+60insTTT...
NM_001122665.2:c.1903+59_1903+60insTTT	NP_001116137.1:n.1903+59_1903+60insTTT
NM_001302552.1:c.1894+59_1894+60insTTT	NP_001289481.1:n.1894+59_1894+60insTTT
NM_004660.4:c.1903+59_1903+60insTTT	NP_004651.2:n.1903+59_1903+60insTTT
XM_006724878.1:c.1834+59_1834+60insTTT	XP_006724941.1:n.1834+59_1834+60insTTT
NM_001122665.3:c.1903+59_1903+60insTTT	NP_001116137.1:n.1903+59_1903+60insTTT
NM_001302552.2:c.1894+59_1894+60insTTT	NP_001289481.1:n.1894+59_1894+60insTTT
NM_001324195.1:c.1834+59_1834+60insTTT	NP_001311124.1:n.1834+59_1834+60insTTT
NR_136716.1:n.2372+59_2372+60insTTT
NR_136717.1:n.2134+59_2134+60insTTT
NR_136718.1:n.2452+59_2452+60insTTT
NR_136719.1:n.2242+59_2242+60insTTT
NR_136720.1:n.2303+59_2303+60insTTT
NR_136721.1:n.1965+59_1965+60insTTT
NR_136722.1:n.2049+59_2049+60insTTT
NR_136723.1:n.2367+59_2367+60insTTT
NR_136724.1:n.2287+59_2287+60insTTT
XR_001756014.2:n.2067+59_2067+60insTTT
NM_004660.5:c.1903+59_1903+60insTTT MANE Select	NP_004651.2:n.1903+59_1903+60insTTT
NM_001302552.3:c.1894+59_1894+60insTTT	NP_001289481.1:n.1894+59_1894+60insTTT
NM_001324195.2:c.1834+59_1834+60insTTT	NP_001311124.1:n.1834+59_1834+60insTTT
NR_136716.2:n.2290+59_2290+60insTTT
NR_136717.2:n.2052+59_2052+60insTTT
NR_136718.2:n.2370+59_2370+60insTTT
NR_136719.2:n.2160+59_2160+60insTTT
NR_136720.2:n.2221+59_2221+60insTTT
NR_136721.2:n.1955+59_1955+60insTTT