Canonical Allele Identifier: CA414987662

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027651A>C (hg19) ; chrY:g.12915739A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915739A>C , CM000686.2:g.12915739A>C	GRCh38
NC_000024.9:g.15027651A>C , CM000686.1:g.15027651A>C	GRCh37
NC_000024.8:g.13537045A>C	NCBI36
NG_012831.1:g.16633A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1129A>C MANE Select	ENSP00000336725.3:p.Met377Leu
ENST00000336079.7:c.1129A>C	ENSP00000336725.3:p.Met377Leu
ENST00000360160.8:c.1129A>C	ENSP00000353284.4:p.Met377Leu
ENST00000495478.1:n.244A>C
NM_001122665.2:c.1129A>C	NP_001116137.1:p.Met377Leu
NM_001302552.1:c.1120A>C	NP_001289481.1:p.Met374Leu
NM_004660.4:c.1129A>C	NP_004651.2:p.Met377Leu
XM_006724878.1:c.1129A>C	XP_006724941.1:p.Met377Leu
XM_011531471.1:c.1129A>C	XP_011529773.1:p.Met377Leu
NM_001122665.3:c.1129A>C	NP_001116137.1:p.Met377Leu
NM_001302552.2:c.1120A>C	NP_001289481.1:p.Met374Leu
NM_001324195.1:c.1129A>C	NP_001311124.1:p.Met377Leu
NR_136716.1:n.1598A>C
NR_136717.1:n.1360A>C
NR_136718.1:n.1678A>C
NR_136719.1:n.1468A>C
NR_136720.1:n.1598A>C
NR_136721.1:n.1191A>C
NR_136722.1:n.1275A>C
NR_136723.1:n.1593A>C
NR_136724.1:n.1513A>C
XR_001756014.2:n.1233A>C
NM_004660.5:c.1129A>C MANE Select	NP_004651.2:p.Met377Leu
NM_001302552.3:c.1120A>C	NP_001289481.1:p.Met374Leu
NM_001324195.2:c.1129A>C	NP_001311124.1:p.Met377Leu
NR_136716.2:n.1516A>C
NR_136717.2:n.1278A>C
NR_136718.2:n.1596A>C
NR_136719.2:n.1386A>C
NR_136720.2:n.1516A>C
NR_136721.2:n.1181A>C