Canonical Allele Identifier: CA2277047800

Gene: DNAH17

Linked Data

• dbSNP Id: rs2092278472

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78567014_78567015insT , CM000679.2:g.78567014_78567015insT	GRCh38
NC_000017.10:g.76563096_76563097insT , CM000679.1:g.76563096_76563097insT	GRCh37
NC_000017.9:g.74074691_74074692insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389840.7:c.1436_1437insA MANE Select	ENSP00000374490.6:p.Asp480GlyfsTer8
ENST00000389840.6:c.1436_1437insA	ENSP00000374490.6:p.Asp480GlyfsTer8
ENST00000585328.5:c.1436_1437insA	ENSP00000465516.1:p.Asp480GlyfsTer8
ENST00000589793.1:n.648_649insA
NM_173628.3:c.1436_1437insA	NP_775899.3:p.Asp480GlyfsTer8
XM_011525416.1:c.1436_1437insA	XP_011523718.1:p.Asp480GlyfsTer8
XM_011525417.1:c.1436_1437insA	XP_011523719.1:p.Asp480GlyfsTer8
XR_934583.1:n.1597_1598insA
XM_011525416.2:c.1436_1437insA	XP_011523718.1:p.Asp480GlyfsTer8
XM_024451013.1:c.1436_1437insA	XP_024306781.1:p.Asp480GlyfsTer8
XM_024451014.1:c.1436_1437insA	XP_024306782.1:p.Asp480GlyfsTer8
XR_002958080.1:n.1599_1600insA
XR_002958081.1:n.1603_1604insA
NM_173628.4:c.1436_1437insA MANE Select	NP_775899.3:p.Asp480GlyfsTer8