Canonical Allele Identifier: CA519895905

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15025665G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12913753G>C , CM000686.2:g.12913753G>C	GRCh38
NC_000024.9:g.15025665G>C , CM000686.1:g.15025665G>C	GRCh37
NC_000024.8:g.13535059G>C	NCBI36
NG_012831.1:g.14647G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.573G>C MANE Select	ENSP00000336725.3:p.Gly191=
ENST00000336079.7:c.573G>C	ENSP00000336725.3:p.Gly191=
ENST00000360160.8:c.573G>C	ENSP00000353284.4:p.Gly191=
ENST00000440554.1:c.564G>C	ENSP00000400377.1:p.Gly188=
ENST00000454054.5:c.573G>C	ENSP00000398953.1:p.Gly191=
ENST00000463199.1:n.91G>C
ENST00000469101.1:n.459G>C
ENST00000472510.5:n.136G>C
NM_001122665.2:c.573G>C	NP_001116137.1:p.Gly191=
NM_001302552.1:c.564G>C	NP_001289481.1:p.Gly188=
NM_004660.4:c.573G>C	NP_004651.2:p.Gly191=
XM_006724878.1:c.573G>C	XP_006724941.1:p.Gly191=
XM_011531471.1:c.573G>C	XP_011529773.1:p.Gly191=
NM_001122665.3:c.573G>C	NP_001116137.1:p.Gly191=
NM_001302552.2:c.564G>C	NP_001289481.1:p.Gly188=
NM_001324195.1:c.573G>C	NP_001311124.1:p.Gly191=
NR_136716.1:n.724G>C
NR_136717.1:n.804G>C
NR_136718.1:n.804G>C
NR_136719.1:n.594G>C
NR_136720.1:n.724G>C
NR_136721.1:n.652G>C
NR_136722.1:n.719G>C
NR_136723.1:n.719G>C
NR_136724.1:n.639G>C
XR_001756014.2:n.677G>C
NM_004660.5:c.573G>C MANE Select	NP_004651.2:p.Gly191=
NM_001302552.3:c.564G>C	NP_001289481.1:p.Gly188=
NM_001324195.2:c.573G>C	NP_001311124.1:p.Gly191=
NR_136716.2:n.642G>C
NR_136717.2:n.722G>C
NR_136718.2:n.722G>C
NR_136719.2:n.512G>C
NR_136720.2:n.642G>C
NR_136721.2:n.642G>C