Canonical Allele Identifier: CA414987216

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027572G>C (hg19) ; chrY:g.12915660G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915660G>C , CM000686.2:g.12915660G>C	GRCh38
NC_000024.9:g.15027572G>C , CM000686.1:g.15027572G>C	GRCh37
NC_000024.8:g.13536966G>C	NCBI36
NG_012831.1:g.16554G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1050G>C MANE Select	ENSP00000336725.3:p.Met350Ile
ENST00000336079.7:c.1050G>C	ENSP00000336725.3:p.Met350Ile
ENST00000360160.8:c.1050G>C	ENSP00000353284.4:p.Met350Ile
ENST00000495478.1:n.165G>C
NM_001122665.2:c.1050G>C	NP_001116137.1:p.Met350Ile
NM_001302552.1:c.1041G>C	NP_001289481.1:p.Met347Ile
NM_004660.4:c.1050G>C	NP_004651.2:p.Met350Ile
XM_006724878.1:c.1050G>C	XP_006724941.1:p.Met350Ile
XM_011531471.1:c.1050G>C	XP_011529773.1:p.Met350Ile
NM_001122665.3:c.1050G>C	NP_001116137.1:p.Met350Ile
NM_001302552.2:c.1041G>C	NP_001289481.1:p.Met347Ile
NM_001324195.1:c.1050G>C	NP_001311124.1:p.Met350Ile
NR_136716.1:n.1519G>C
NR_136717.1:n.1281G>C
NR_136718.1:n.1599G>C
NR_136719.1:n.1389G>C
NR_136720.1:n.1519G>C
NR_136721.1:n.1112G>C
NR_136722.1:n.1196G>C
NR_136723.1:n.1514G>C
NR_136724.1:n.1434G>C
XR_001756014.2:n.1154G>C
NM_004660.5:c.1050G>C MANE Select	NP_004651.2:p.Met350Ile
NM_001302552.3:c.1041G>C	NP_001289481.1:p.Met347Ile
NM_001324195.2:c.1050G>C	NP_001311124.1:p.Met350Ile
NR_136716.2:n.1437G>C
NR_136717.2:n.1199G>C
NR_136718.2:n.1517G>C
NR_136719.2:n.1307G>C
NR_136720.2:n.1437G>C
NR_136721.2:n.1102G>C