Canonical Allele Identifier: CA414987670

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027652T>C (hg19) ; chrY:g.12915740T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915740T>C , CM000686.2:g.12915740T>C	GRCh38
NC_000024.9:g.15027652T>C , CM000686.1:g.15027652T>C	GRCh37
NC_000024.8:g.13537046T>C	NCBI36
NG_012831.1:g.16634T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1130T>C MANE Select	ENSP00000336725.3:p.Met377Thr
ENST00000336079.7:c.1130T>C	ENSP00000336725.3:p.Met377Thr
ENST00000360160.8:c.1130T>C	ENSP00000353284.4:p.Met377Thr
ENST00000495478.1:n.245T>C
NM_001122665.2:c.1130T>C	NP_001116137.1:p.Met377Thr
NM_001302552.1:c.1121T>C	NP_001289481.1:p.Met374Thr
NM_004660.4:c.1130T>C	NP_004651.2:p.Met377Thr
XM_006724878.1:c.1130T>C	XP_006724941.1:p.Met377Thr
XM_011531471.1:c.1130T>C	XP_011529773.1:p.Met377Thr
NM_001122665.3:c.1130T>C	NP_001116137.1:p.Met377Thr
NM_001302552.2:c.1121T>C	NP_001289481.1:p.Met374Thr
NM_001324195.1:c.1130T>C	NP_001311124.1:p.Met377Thr
NR_136716.1:n.1599T>C
NR_136717.1:n.1361T>C
NR_136718.1:n.1679T>C
NR_136719.1:n.1469T>C
NR_136720.1:n.1599T>C
NR_136721.1:n.1192T>C
NR_136722.1:n.1276T>C
NR_136723.1:n.1594T>C
NR_136724.1:n.1514T>C
XR_001756014.2:n.1234T>C
NM_004660.5:c.1130T>C MANE Select	NP_004651.2:p.Met377Thr
NM_001302552.3:c.1121T>C	NP_001289481.1:p.Met374Thr
NM_001324195.2:c.1130T>C	NP_001311124.1:p.Met377Thr
NR_136716.2:n.1517T>C
NR_136717.2:n.1279T>C
NR_136718.2:n.1597T>C
NR_136719.2:n.1387T>C
NR_136720.2:n.1517T>C
NR_136721.2:n.1182T>C