Canonical Allele Identifier: CA414992683

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15029402C>G (hg19) ; chrY:g.12917490C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917490C>G , CM000686.2:g.12917490C>G	GRCh38
NC_000024.9:g.15029402C>G , CM000686.1:g.15029402C>G	GRCh37
NC_000024.8:g.13538796C>G	NCBI36
NG_012831.1:g.18384C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1851C>G MANE Select	ENSP00000336725.3:p.Ser617Arg
ENST00000336079.7:c.1851C>G	ENSP00000336725.3:p.Ser617Arg
ENST00000360160.8:c.1851C>G	ENSP00000353284.4:p.Ser617Arg
NM_001122665.2:c.1851C>G	NP_001116137.1:p.Ser617Arg
NM_001302552.1:c.1842C>G	NP_001289481.1:p.Ser614Arg
NM_004660.4:c.1851C>G	NP_004651.2:p.Ser617Arg
XM_006724878.1:c.1782C>G	XP_006724941.1:p.Ser594Arg
NM_001122665.3:c.1851C>G	NP_001116137.1:p.Ser617Arg
NM_001302552.2:c.1842C>G	NP_001289481.1:p.Ser614Arg
NM_001324195.1:c.1782C>G	NP_001311124.1:p.Ser594Arg
NR_136716.1:n.2320C>G
NR_136717.1:n.2082C>G
NR_136718.1:n.2400C>G
NR_136719.1:n.2190C>G
NR_136720.1:n.2251C>G
NR_136721.1:n.1913C>G
NR_136722.1:n.1997C>G
NR_136723.1:n.2315C>G
NR_136724.1:n.2235C>G
XR_001756014.2:n.2015C>G
NM_004660.5:c.1851C>G MANE Select	NP_004651.2:p.Ser617Arg
NM_001302552.3:c.1842C>G	NP_001289481.1:p.Ser614Arg
NM_001324195.2:c.1782C>G	NP_001311124.1:p.Ser594Arg
NR_136716.2:n.2238C>G
NR_136717.2:n.2000C>G
NR_136718.2:n.2318C>G
NR_136719.2:n.2108C>G
NR_136720.2:n.2169C>G
NR_136721.2:n.1903C>G