Canonical Allele Identifier: CA414987203

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027570A>T (hg19) ; chrY:g.12915658A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915658A>T , CM000686.2:g.12915658A>T	GRCh38
NC_000024.9:g.15027570A>T , CM000686.1:g.15027570A>T	GRCh37
NC_000024.8:g.13536964A>T	NCBI36
NG_012831.1:g.16552A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1048A>T MANE Select	ENSP00000336725.3:p.Met350Leu
ENST00000336079.7:c.1048A>T	ENSP00000336725.3:p.Met350Leu
ENST00000360160.8:c.1048A>T	ENSP00000353284.4:p.Met350Leu
ENST00000495478.1:n.163A>T
NM_001122665.2:c.1048A>T	NP_001116137.1:p.Met350Leu
NM_001302552.1:c.1039A>T	NP_001289481.1:p.Met347Leu
NM_004660.4:c.1048A>T	NP_004651.2:p.Met350Leu
XM_006724878.1:c.1048A>T	XP_006724941.1:p.Met350Leu
XM_011531471.1:c.1048A>T	XP_011529773.1:p.Met350Leu
NM_001122665.3:c.1048A>T	NP_001116137.1:p.Met350Leu
NM_001302552.2:c.1039A>T	NP_001289481.1:p.Met347Leu
NM_001324195.1:c.1048A>T	NP_001311124.1:p.Met350Leu
NR_136716.1:n.1517A>T
NR_136717.1:n.1279A>T
NR_136718.1:n.1597A>T
NR_136719.1:n.1387A>T
NR_136720.1:n.1517A>T
NR_136721.1:n.1110A>T
NR_136722.1:n.1194A>T
NR_136723.1:n.1512A>T
NR_136724.1:n.1432A>T
XR_001756014.2:n.1152A>T
NM_004660.5:c.1048A>T MANE Select	NP_004651.2:p.Met350Leu
NM_001302552.3:c.1039A>T	NP_001289481.1:p.Met347Leu
NM_001324195.2:c.1048A>T	NP_001311124.1:p.Met350Leu
NR_136716.2:n.1435A>T
NR_136717.2:n.1197A>T
NR_136718.2:n.1515A>T
NR_136719.2:n.1305A>T
NR_136720.2:n.1435A>T
NR_136721.2:n.1100A>T