Canonical Allele Identifier: CA414987676

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027653G>C (hg19) ; chrY:g.12915741G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915741G>C , CM000686.2:g.12915741G>C	GRCh38
NC_000024.9:g.15027653G>C , CM000686.1:g.15027653G>C	GRCh37
NC_000024.8:g.13537047G>C	NCBI36
NG_012831.1:g.16635G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1131G>C MANE Select	ENSP00000336725.3:p.Met377Ile
ENST00000336079.7:c.1131G>C	ENSP00000336725.3:p.Met377Ile
ENST00000360160.8:c.1131G>C	ENSP00000353284.4:p.Met377Ile
ENST00000495478.1:n.246G>C
NM_001122665.2:c.1131G>C	NP_001116137.1:p.Met377Ile
NM_001302552.1:c.1122G>C	NP_001289481.1:p.Met374Ile
NM_004660.4:c.1131G>C	NP_004651.2:p.Met377Ile
XM_006724878.1:c.1131G>C	XP_006724941.1:p.Met377Ile
XM_011531471.1:c.1131G>C	XP_011529773.1:p.Met377Ile
NM_001122665.3:c.1131G>C	NP_001116137.1:p.Met377Ile
NM_001302552.2:c.1122G>C	NP_001289481.1:p.Met374Ile
NM_001324195.1:c.1131G>C	NP_001311124.1:p.Met377Ile
NR_136716.1:n.1600G>C
NR_136717.1:n.1362G>C
NR_136718.1:n.1680G>C
NR_136719.1:n.1470G>C
NR_136720.1:n.1600G>C
NR_136721.1:n.1193G>C
NR_136722.1:n.1277G>C
NR_136723.1:n.1595G>C
NR_136724.1:n.1515G>C
XR_001756014.2:n.1235G>C
NM_004660.5:c.1131G>C MANE Select	NP_004651.2:p.Met377Ile
NM_001302552.3:c.1122G>C	NP_001289481.1:p.Met374Ile
NM_001324195.2:c.1131G>C	NP_001311124.1:p.Met377Ile
NR_136716.2:n.1518G>C
NR_136717.2:n.1280G>C
NR_136718.2:n.1598G>C
NR_136719.2:n.1388G>C
NR_136720.2:n.1518G>C
NR_136721.2:n.1183G>C