Canonical Allele Identifier: CA519895658

Gene: DDX3Y

Linked Data

• gnomAD v3: Y-12913726-T-C
• gnomAD v4: Y-12913726-T-C
• MyVariant Identifiers: chrY:g.15025638T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12913726T>C , CM000686.2:g.12913726T>C	GRCh38
NC_000024.9:g.15025638T>C , CM000686.1:g.15025638T>C	GRCh37
NC_000024.8:g.13535032T>C	NCBI36
NG_012831.1:g.14620T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.546T>C MANE Select	ENSP00000336725.3:p.Asp182=
ENST00000336079.7:c.546T>C	ENSP00000336725.3:p.Asp182=
ENST00000360160.8:c.546T>C	ENSP00000353284.4:p.Asp182=
ENST00000440554.1:c.537T>C	ENSP00000400377.1:p.Asp179=
ENST00000454054.5:c.546T>C	ENSP00000398953.1:p.Asp182=
ENST00000463199.1:n.64T>C
ENST00000469101.1:n.432T>C
ENST00000472510.5:n.109T>C
NM_001122665.2:c.546T>C	NP_001116137.1:p.Asp182=
NM_001302552.1:c.537T>C	NP_001289481.1:p.Asp179=
NM_004660.4:c.546T>C	NP_004651.2:p.Asp182=
XM_006724878.1:c.546T>C	XP_006724941.1:p.Asp182=
XM_011531471.1:c.546T>C	XP_011529773.1:p.Asp182=
NM_001122665.3:c.546T>C	NP_001116137.1:p.Asp182=
NM_001302552.2:c.537T>C	NP_001289481.1:p.Asp179=
NM_001324195.1:c.546T>C	NP_001311124.1:p.Asp182=
NR_136716.1:n.697T>C
NR_136717.1:n.777T>C
NR_136718.1:n.777T>C
NR_136719.1:n.567T>C
NR_136720.1:n.697T>C
NR_136721.1:n.625T>C
NR_136722.1:n.692T>C
NR_136723.1:n.692T>C
NR_136724.1:n.612T>C
XR_001756014.2:n.650T>C
NM_004660.5:c.546T>C MANE Select	NP_004651.2:p.Asp182=
NM_001302552.3:c.537T>C	NP_001289481.1:p.Asp179=
NM_001324195.2:c.546T>C	NP_001311124.1:p.Asp182=
NR_136716.2:n.615T>C
NR_136717.2:n.695T>C
NR_136718.2:n.695T>C
NR_136719.2:n.485T>C
NR_136720.2:n.615T>C
NR_136721.2:n.615T>C