Canonical Allele Identifier: CA520499212

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027674T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915762T>A , CM000686.2:g.12915762T>A	GRCh38
NC_000024.9:g.15027674T>A , CM000686.1:g.15027674T>A	GRCh37
NC_000024.8:g.13537068T>A	NCBI36
NG_012831.1:g.16656T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1152T>A MANE Select	ENSP00000336725.3:p.Pro384=
ENST00000336079.7:c.1152T>A	ENSP00000336725.3:p.Pro384=
ENST00000360160.8:c.1152T>A	ENSP00000353284.4:p.Pro384=
ENST00000495478.1:n.267T>A
NM_001122665.2:c.1152T>A	NP_001116137.1:p.Pro384=
NM_001302552.1:c.1143T>A	NP_001289481.1:p.Pro381=
NM_004660.4:c.1152T>A	NP_004651.2:p.Pro384=
XM_006724878.1:c.1152T>A	XP_006724941.1:p.Pro384=
XM_011531471.1:c.1152T>A	XP_011529773.1:p.Pro384=
NM_001122665.3:c.1152T>A	NP_001116137.1:p.Pro384=
NM_001302552.2:c.1143T>A	NP_001289481.1:p.Pro381=
NM_001324195.1:c.1152T>A	NP_001311124.1:p.Pro384=
NR_136716.1:n.1621T>A
NR_136717.1:n.1383T>A
NR_136718.1:n.1701T>A
NR_136719.1:n.1491T>A
NR_136720.1:n.1621T>A
NR_136721.1:n.1214T>A
NR_136722.1:n.1298T>A
NR_136723.1:n.1616T>A
NR_136724.1:n.1536T>A
XR_001756014.2:n.1256T>A
NM_004660.5:c.1152T>A MANE Select	NP_004651.2:p.Pro384=
NM_001302552.3:c.1143T>A	NP_001289481.1:p.Pro381=
NM_001324195.2:c.1152T>A	NP_001311124.1:p.Pro384=
NR_136716.2:n.1539T>A
NR_136717.2:n.1301T>A
NR_136718.2:n.1619T>A
NR_136719.2:n.1409T>A
NR_136720.2:n.1539T>A
NR_136721.2:n.1204T>A