Canonical Allele Identifier: CA414987651

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027649C>G (hg19) ; chrY:g.12915737C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915737C>G , CM000686.2:g.12915737C>G	GRCh38
NC_000024.9:g.15027649C>G , CM000686.1:g.15027649C>G	GRCh37
NC_000024.8:g.13537043C>G	NCBI36
NG_012831.1:g.16631C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1127C>G MANE Select	ENSP00000336725.3:p.Thr376Ser
ENST00000336079.7:c.1127C>G	ENSP00000336725.3:p.Thr376Ser
ENST00000360160.8:c.1127C>G	ENSP00000353284.4:p.Thr376Ser
ENST00000495478.1:n.242C>G
NM_001122665.2:c.1127C>G	NP_001116137.1:p.Thr376Ser
NM_001302552.1:c.1118C>G	NP_001289481.1:p.Thr373Ser
NM_004660.4:c.1127C>G	NP_004651.2:p.Thr376Ser
XM_006724878.1:c.1127C>G	XP_006724941.1:p.Thr376Ser
XM_011531471.1:c.1127C>G	XP_011529773.1:p.Thr376Ser
NM_001122665.3:c.1127C>G	NP_001116137.1:p.Thr376Ser
NM_001302552.2:c.1118C>G	NP_001289481.1:p.Thr373Ser
NM_001324195.1:c.1127C>G	NP_001311124.1:p.Thr376Ser
NR_136716.1:n.1596C>G
NR_136717.1:n.1358C>G
NR_136718.1:n.1676C>G
NR_136719.1:n.1466C>G
NR_136720.1:n.1596C>G
NR_136721.1:n.1189C>G
NR_136722.1:n.1273C>G
NR_136723.1:n.1591C>G
NR_136724.1:n.1511C>G
XR_001756014.2:n.1231C>G
NM_004660.5:c.1127C>G MANE Select	NP_004651.2:p.Thr376Ser
NM_001302552.3:c.1118C>G	NP_001289481.1:p.Thr373Ser
NM_001324195.2:c.1127C>G	NP_001311124.1:p.Thr376Ser
NR_136716.2:n.1514C>G
NR_136717.2:n.1276C>G
NR_136718.2:n.1594C>G
NR_136719.2:n.1384C>G
NR_136720.2:n.1514C>G
NR_136721.2:n.1179C>G