Canonical Allele Identifier: CA414984433

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15026498T>G (hg19) ; chrY:g.12914586T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914586T>G , CM000686.2:g.12914586T>G	GRCh38
NC_000024.9:g.15026498T>G , CM000686.1:g.15026498T>G	GRCh37
NC_000024.8:g.13535892T>G	NCBI36
NG_012831.1:g.15480T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.696T>G MANE Select	ENSP00000336725.3:p.Phe232Leu
ENST00000336079.7:c.696T>G	ENSP00000336725.3:p.Phe232Leu
ENST00000360160.8:c.696T>G	ENSP00000353284.4:p.Phe232Leu
ENST00000440554.1:c.687T>G	ENSP00000400377.1:p.Phe229Leu
ENST00000463199.1:n.214T>G
ENST00000472510.5:n.259T>G
NM_001122665.2:c.696T>G	NP_001116137.1:p.Phe232Leu
NM_001302552.1:c.687T>G	NP_001289481.1:p.Phe229Leu
NM_004660.4:c.696T>G	NP_004651.2:p.Phe232Leu
XM_006724878.1:c.696T>G	XP_006724941.1:p.Phe232Leu
XM_011531471.1:c.696T>G	XP_011529773.1:p.Phe232Leu
NM_001122665.3:c.696T>G	NP_001116137.1:p.Phe232Leu
NM_001302552.2:c.687T>G	NP_001289481.1:p.Phe229Leu
NM_001324195.1:c.696T>G	NP_001311124.1:p.Phe232Leu
NR_136716.1:n.847T>G
NR_136717.1:n.927T>G
NR_136718.1:n.927T>G
NR_136719.1:n.717T>G
NR_136720.1:n.847T>G
NR_136721.1:n.775T>G
NR_136722.1:n.842T>G
NR_136723.1:n.842T>G
NR_136724.1:n.762T>G
XR_001756014.2:n.800T>G
NM_004660.5:c.696T>G MANE Select	NP_004651.2:p.Phe232Leu
NM_001302552.3:c.687T>G	NP_001289481.1:p.Phe229Leu
NM_001324195.2:c.696T>G	NP_001311124.1:p.Phe232Leu
NR_136716.2:n.765T>G
NR_136717.2:n.845T>G
NR_136718.2:n.845T>G
NR_136719.2:n.635T>G
NR_136720.2:n.765T>G
NR_136721.2:n.765T>G