Canonical Allele Identifier: CA414987300

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027586T>C (hg19) ; chrY:g.12915674T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915674T>C , CM000686.2:g.12915674T>C	GRCh38
NC_000024.9:g.15027586T>C , CM000686.1:g.15027586T>C	GRCh37
NC_000024.8:g.13536980T>C	NCBI36
NG_012831.1:g.16568T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1064T>C MANE Select	ENSP00000336725.3:p.Phe355Ser
ENST00000336079.7:c.1064T>C	ENSP00000336725.3:p.Phe355Ser
ENST00000360160.8:c.1064T>C	ENSP00000353284.4:p.Phe355Ser
ENST00000495478.1:n.179T>C
NM_001122665.2:c.1064T>C	NP_001116137.1:p.Phe355Ser
NM_001302552.1:c.1055T>C	NP_001289481.1:p.Phe352Ser
NM_004660.4:c.1064T>C	NP_004651.2:p.Phe355Ser
XM_006724878.1:c.1064T>C	XP_006724941.1:p.Phe355Ser
XM_011531471.1:c.1064T>C	XP_011529773.1:p.Phe355Ser
NM_001122665.3:c.1064T>C	NP_001116137.1:p.Phe355Ser
NM_001302552.2:c.1055T>C	NP_001289481.1:p.Phe352Ser
NM_001324195.1:c.1064T>C	NP_001311124.1:p.Phe355Ser
NR_136716.1:n.1533T>C
NR_136717.1:n.1295T>C
NR_136718.1:n.1613T>C
NR_136719.1:n.1403T>C
NR_136720.1:n.1533T>C
NR_136721.1:n.1126T>C
NR_136722.1:n.1210T>C
NR_136723.1:n.1528T>C
NR_136724.1:n.1448T>C
XR_001756014.2:n.1168T>C
NM_004660.5:c.1064T>C MANE Select	NP_004651.2:p.Phe355Ser
NM_001302552.3:c.1055T>C	NP_001289481.1:p.Phe352Ser
NM_001324195.2:c.1064T>C	NP_001311124.1:p.Phe355Ser
NR_136716.2:n.1451T>C
NR_136717.2:n.1213T>C
NR_136718.2:n.1531T>C
NR_136719.2:n.1321T>C
NR_136720.2:n.1451T>C
NR_136721.2:n.1116T>C