Canonical Allele Identifier: CA414987954

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027801G>T (hg19) ; chrY:g.12915889G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915889G>T , CM000686.2:g.12915889G>T	GRCh38
NC_000024.9:g.15027801G>T , CM000686.1:g.15027801G>T	GRCh37
NC_000024.8:g.13537195G>T	NCBI36
NG_012831.1:g.16783G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1171G>T MANE Select	ENSP00000336725.3:p.Ala391Ser
ENST00000336079.7:c.1171G>T	ENSP00000336725.3:p.Ala391Ser
ENST00000360160.8:c.1171G>T	ENSP00000353284.4:p.Ala391Ser
ENST00000495478.1:n.286G>T
NM_001122665.2:c.1171G>T	NP_001116137.1:p.Ala391Ser
NM_001302552.1:c.1162G>T	NP_001289481.1:p.Ala388Ser
NM_004660.4:c.1171G>T	NP_004651.2:p.Ala391Ser
XM_006724878.1:c.1171G>T	XP_006724941.1:p.Ala391Ser
XM_011531471.1:c.1171G>T	XP_011529773.1:p.Ala391Ser
NM_001122665.3:c.1171G>T	NP_001116137.1:p.Ala391Ser
NM_001302552.2:c.1162G>T	NP_001289481.1:p.Ala388Ser
NM_001324195.1:c.1171G>T	NP_001311124.1:p.Ala391Ser
NR_136716.1:n.1640G>T
NR_136717.1:n.1402G>T
NR_136718.1:n.1720G>T
NR_136719.1:n.1510G>T
NR_136720.1:n.1640G>T
NR_136721.1:n.1233G>T
NR_136722.1:n.1317G>T
NR_136723.1:n.1635G>T
NR_136724.1:n.1555G>T
XR_001756014.2:n.1275G>T
NM_004660.5:c.1171G>T MANE Select	NP_004651.2:p.Ala391Ser
NM_001302552.3:c.1162G>T	NP_001289481.1:p.Ala388Ser
NM_001324195.2:c.1171G>T	NP_001311124.1:p.Ala391Ser
NR_136716.2:n.1558G>T
NR_136717.2:n.1320G>T
NR_136718.2:n.1638G>T
NR_136719.2:n.1428G>T
NR_136720.2:n.1558G>T
NR_136721.2:n.1223G>T