Canonical Allele Identifier: CA414984293

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15026478T>C (hg19) ; chrY:g.12914566T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914566T>C , CM000686.2:g.12914566T>C	GRCh38
NC_000024.9:g.15026478T>C , CM000686.1:g.15026478T>C	GRCh37
NC_000024.8:g.13535872T>C	NCBI36
NG_012831.1:g.15460T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.676T>C MANE Select	ENSP00000336725.3:p.Ser226Pro
ENST00000336079.7:c.676T>C	ENSP00000336725.3:p.Ser226Pro
ENST00000360160.8:c.676T>C	ENSP00000353284.4:p.Ser226Pro
ENST00000440554.1:c.667T>C	ENSP00000400377.1:p.Ser223Pro
ENST00000463199.1:n.194T>C
ENST00000472510.5:n.239T>C
NM_001122665.2:c.676T>C	NP_001116137.1:p.Ser226Pro
NM_001302552.1:c.667T>C	NP_001289481.1:p.Ser223Pro
NM_004660.4:c.676T>C	NP_004651.2:p.Ser226Pro
XM_006724878.1:c.676T>C	XP_006724941.1:p.Ser226Pro
XM_011531471.1:c.676T>C	XP_011529773.1:p.Ser226Pro
NM_001122665.3:c.676T>C	NP_001116137.1:p.Ser226Pro
NM_001302552.2:c.667T>C	NP_001289481.1:p.Ser223Pro
NM_001324195.1:c.676T>C	NP_001311124.1:p.Ser226Pro
NR_136716.1:n.827T>C
NR_136717.1:n.907T>C
NR_136718.1:n.907T>C
NR_136719.1:n.697T>C
NR_136720.1:n.827T>C
NR_136721.1:n.755T>C
NR_136722.1:n.822T>C
NR_136723.1:n.822T>C
NR_136724.1:n.742T>C
XR_001756014.2:n.780T>C
NM_004660.5:c.676T>C MANE Select	NP_004651.2:p.Ser226Pro
NM_001302552.3:c.667T>C	NP_001289481.1:p.Ser223Pro
NM_001324195.2:c.676T>C	NP_001311124.1:p.Ser226Pro
NR_136716.2:n.745T>C
NR_136717.2:n.825T>C
NR_136718.2:n.825T>C
NR_136719.2:n.615T>C
NR_136720.2:n.745T>C
NR_136721.2:n.745T>C