Canonical Allele Identifier: CA520498271

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027573C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915661C>T , CM000686.2:g.12915661C>T	GRCh38
NC_000024.9:g.15027573C>T , CM000686.1:g.15027573C>T	GRCh37
NC_000024.8:g.13536967C>T	NCBI36
NG_012831.1:g.16555C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1051C>T MANE Select	ENSP00000336725.3:p.Leu351=
ENST00000336079.7:c.1051C>T	ENSP00000336725.3:p.Leu351=
ENST00000360160.8:c.1051C>T	ENSP00000353284.4:p.Leu351=
ENST00000495478.1:n.166C>T
NM_001122665.2:c.1051C>T	NP_001116137.1:p.Leu351=
NM_001302552.1:c.1042C>T	NP_001289481.1:p.Leu348=
NM_004660.4:c.1051C>T	NP_004651.2:p.Leu351=
XM_006724878.1:c.1051C>T	XP_006724941.1:p.Leu351=
XM_011531471.1:c.1051C>T	XP_011529773.1:p.Leu351=
NM_001122665.3:c.1051C>T	NP_001116137.1:p.Leu351=
NM_001302552.2:c.1042C>T	NP_001289481.1:p.Leu348=
NM_001324195.1:c.1051C>T	NP_001311124.1:p.Leu351=
NR_136716.1:n.1520C>T
NR_136717.1:n.1282C>T
NR_136718.1:n.1600C>T
NR_136719.1:n.1390C>T
NR_136720.1:n.1520C>T
NR_136721.1:n.1113C>T
NR_136722.1:n.1197C>T
NR_136723.1:n.1515C>T
NR_136724.1:n.1435C>T
XR_001756014.2:n.1155C>T
NM_004660.5:c.1051C>T MANE Select	NP_004651.2:p.Leu351=
NM_001302552.3:c.1042C>T	NP_001289481.1:p.Leu348=
NM_001324195.2:c.1051C>T	NP_001311124.1:p.Leu351=
NR_136716.2:n.1438C>T
NR_136717.2:n.1200C>T
NR_136718.2:n.1518C>T
NR_136719.2:n.1308C>T
NR_136720.2:n.1438C>T
NR_136721.2:n.1103C>T