Canonical Allele Identifier: CA414987986

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027809C>G (hg19) ; chrY:g.12915897C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915897C>G , CM000686.2:g.12915897C>G	GRCh38
NC_000024.9:g.15027809C>G , CM000686.1:g.15027809C>G	GRCh37
NC_000024.8:g.13537203C>G	NCBI36
NG_012831.1:g.16791C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1179C>G MANE Select	ENSP00000336725.3:p.Asp393Glu
ENST00000336079.7:c.1179C>G	ENSP00000336725.3:p.Asp393Glu
ENST00000360160.8:c.1179C>G	ENSP00000353284.4:p.Asp393Glu
ENST00000495478.1:n.294C>G
NM_001122665.2:c.1179C>G	NP_001116137.1:p.Asp393Glu
NM_001302552.1:c.1170C>G	NP_001289481.1:p.Asp390Glu
NM_004660.4:c.1179C>G	NP_004651.2:p.Asp393Glu
XM_006724878.1:c.1179C>G	XP_006724941.1:p.Asp393Glu
XM_011531471.1:c.1179C>G	XP_011529773.1:p.Asp393Glu
NM_001122665.3:c.1179C>G	NP_001116137.1:p.Asp393Glu
NM_001302552.2:c.1170C>G	NP_001289481.1:p.Asp390Glu
NM_001324195.1:c.1179C>G	NP_001311124.1:p.Asp393Glu
NR_136716.1:n.1648C>G
NR_136717.1:n.1410C>G
NR_136718.1:n.1728C>G
NR_136719.1:n.1518C>G
NR_136720.1:n.1648C>G
NR_136721.1:n.1241C>G
NR_136722.1:n.1325C>G
NR_136723.1:n.1643C>G
NR_136724.1:n.1563C>G
XR_001756014.2:n.1283C>G
NM_004660.5:c.1179C>G MANE Select	NP_004651.2:p.Asp393Glu
NM_001302552.3:c.1170C>G	NP_001289481.1:p.Asp390Glu
NM_001324195.2:c.1179C>G	NP_001311124.1:p.Asp393Glu
NR_136716.2:n.1566C>G
NR_136717.2:n.1328C>G
NR_136718.2:n.1646C>G
NR_136719.2:n.1436C>G
NR_136720.2:n.1566C>G
NR_136721.2:n.1231C>G