Canonical Allele Identifier: CA2579748522

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917583_12917585del , CM000686.2:g.12917583_12917585del	GRCh38
NC_000024.9:g.15029495_15029497del , CM000686.1:g.15029495_15029497del	GRCh37
NC_000024.8:g.13538889_13538891del	NCBI36
NG_012831.1:g.18477_18479del

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1903+41_1903+43del MANE Select	ENSP00000336725.3:n.1903+41_1903+43del
ENST00000336079.7:c.1903+41_1903+43del	ENSP00000336725.3:n.1903+41_1903+43del
ENST00000360160.8:c.1903+41_1903+43del	ENSP00000353284.4:n.1903+41_1903+43del
NM_001122665.2:c.1903+41_1903+43del	NP_001116137.1:n.1903+41_1903+43del
NM_001302552.1:c.1894+41_1894+43del	NP_001289481.1:n.1894+41_1894+43del
NM_004660.4:c.1903+41_1903+43del	NP_004651.2:n.1903+41_1903+43del
XM_006724878.1:c.1834+41_1834+43del	XP_006724941.1:n.1834+41_1834+43del
NM_001122665.3:c.1903+41_1903+43del	NP_001116137.1:n.1903+41_1903+43del
NM_001302552.2:c.1894+41_1894+43del	NP_001289481.1:n.1894+41_1894+43del
NM_001324195.1:c.1834+41_1834+43del	NP_001311124.1:n.1834+41_1834+43del
NR_136716.1:n.2372+41_2372+43del
NR_136717.1:n.2134+41_2134+43del
NR_136718.1:n.2452+41_2452+43del
NR_136719.1:n.2242+41_2242+43del
NR_136720.1:n.2303+41_2303+43del
NR_136721.1:n.1965+41_1965+43del
NR_136722.1:n.2049+41_2049+43del
NR_136723.1:n.2367+41_2367+43del
NR_136724.1:n.2287+41_2287+43del
XR_001756014.2:n.2067+41_2067+43del
NM_004660.5:c.1903+41_1903+43del MANE Select	NP_004651.2:n.1903+41_1903+43del
NM_001302552.3:c.1894+41_1894+43del	NP_001289481.1:n.1894+41_1894+43del
NM_001324195.2:c.1834+41_1834+43del	NP_001311124.1:n.1834+41_1834+43del
NR_136716.2:n.2290+41_2290+43del
NR_136717.2:n.2052+41_2052+43del
NR_136718.2:n.2370+41_2370+43del
NR_136719.2:n.2160+41_2160+43del
NR_136720.2:n.2221+41_2221+43del
NR_136721.2:n.1955+41_1955+43del