Canonical Allele Identifier: CA520498419

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027608A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915696A>T , CM000686.2:g.12915696A>T	GRCh38
NC_000024.9:g.15027608A>T , CM000686.1:g.15027608A>T	GRCh37
NC_000024.8:g.13537002A>T	NCBI36
NG_012831.1:g.16590A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1086A>T MANE Select	ENSP00000336725.3:p.Ile362=
ENST00000336079.7:c.1086A>T	ENSP00000336725.3:p.Ile362=
ENST00000360160.8:c.1086A>T	ENSP00000353284.4:p.Ile362=
ENST00000495478.1:n.201A>T
NM_001122665.2:c.1086A>T	NP_001116137.1:p.Ile362=
NM_001302552.1:c.1077A>T	NP_001289481.1:p.Ile359=
NM_004660.4:c.1086A>T	NP_004651.2:p.Ile362=
XM_006724878.1:c.1086A>T	XP_006724941.1:p.Ile362=
XM_011531471.1:c.1086A>T	XP_011529773.1:p.Ile362=
NM_001122665.3:c.1086A>T	NP_001116137.1:p.Ile362=
NM_001302552.2:c.1077A>T	NP_001289481.1:p.Ile359=
NM_001324195.1:c.1086A>T	NP_001311124.1:p.Ile362=
NR_136716.1:n.1555A>T
NR_136717.1:n.1317A>T
NR_136718.1:n.1635A>T
NR_136719.1:n.1425A>T
NR_136720.1:n.1555A>T
NR_136721.1:n.1148A>T
NR_136722.1:n.1232A>T
NR_136723.1:n.1550A>T
NR_136724.1:n.1470A>T
XR_001756014.2:n.1190A>T
NM_004660.5:c.1086A>T MANE Select	NP_004651.2:p.Ile362=
NM_001302552.3:c.1077A>T	NP_001289481.1:p.Ile359=
NM_001324195.2:c.1086A>T	NP_001311124.1:p.Ile362=
NR_136716.2:n.1473A>T
NR_136717.2:n.1235A>T
NR_136718.2:n.1553A>T
NR_136719.2:n.1343A>T
NR_136720.2:n.1473A>T
NR_136721.2:n.1138A>T