Canonical Allele Identifier: CA2838369262

Gene: DDX10

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108685668C>T , CM000673.2:g.108685668C>T	GRCh38
NC_000011.9:g.108556395C>T , CM000673.1:g.108556395C>T	GRCh37
NC_000011.8:g.108061605C>T	NCBI36
NG_046987.1:g.25644C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686283.1:c.998+370C>T	ENSP00000509891.1:n.998+370C>T
ENST00000686617.1:c.849-3268C>T	ENSP00000510670.1:n.849-3268C>T
ENST00000687072.1:c.849-3268C>T	ENSP00000509365.1:n.849-3268C>T
ENST00000688536.1:n.934-3268C>T
ENST00000688583.1:c.849-3268C>T	ENSP00000508658.1:n.849-3268C>T
ENST00000688976.1:c.849-3268C>T	ENSP00000508895.1:n.849-3268C>T
ENST00000690021.1:c.849-3268C>T	ENSP00000508781.1:n.849-3268C>T
ENST00000693015.1:n.945-3268C>T
ENST00000322536.8:c.849-3268C>T MANE Select	ENSP00000314348.3:n.849-3268C>T
ENST00000648124.1:c.849-3268C>T	ENSP00000497432.1:n.849-3268C>T
ENST00000322536.7:c.849-3268C>T	ENSP00000314348.3:n.849-3268C>T
ENST00000526794.1:c.849-3268C>T	ENSP00000432032.1:n.849-3268C>T
NM_004398.3:c.849-3268C>T	NP_004389.2:n.849-3268C>T
XM_011542646.1:c.849-3268C>T	XP_011540948.1:n.849-3268C>T
NM_004398.4:c.849-3268C>T MANE Select	NP_004389.2:n.849-3268C>T