Canonical Allele Identifier: CA919901997

Gene: DNAH17

Linked Data

• dbSNP Id: rs1568266523

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78567058dup , CM000679.2:g.78567058dup	GRCh38
NC_000017.10:g.76563140dup , CM000679.1:g.76563140dup	GRCh37
NC_000017.9:g.74074735dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000389840.7:c.1395dup MANE Select	ENSP00000374490.6:p.Glu466Ter
ENST00000389840.6:c.1395dup	ENSP00000374490.6:p.Glu466Ter
ENST00000585328.5:c.1395dup	ENSP00000465516.1:p.Glu466Ter
ENST00000589793.1:n.607dup
NM_173628.3:c.1395dup	NP_775899.3:p.Glu466Ter
XM_011525416.1:c.1395dup	XP_011523718.1:p.Glu466Ter
XM_011525417.1:c.1395dup	XP_011523719.1:p.Glu466Ter
XR_934583.1:n.1556dup
XM_011525416.2:c.1395dup	XP_011523718.1:p.Glu466Ter
XM_024451013.1:c.1395dup	XP_024306781.1:p.Glu466Ter
XM_024451014.1:c.1395dup	XP_024306782.1:p.Glu466Ter
XR_002958080.1:n.1558dup
XR_002958081.1:n.1562dup
NM_173628.4:c.1395dup MANE Select	NP_775899.3:p.Glu466Ter