Canonical Allele Identifier: CA2277047791

Gene: DNAH17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78566997_78566998delinsAC , CM000679.2:g.78566997_78566998delinsAC	GRCh38
NC_000017.10:g.76563079_76563080delinsAC , CM000679.1:g.76563079_76563080delinsAC	GRCh37
NC_000017.9:g.74074674_74074675delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389840.7:c.1452+1_1452+2delinsGT MANE Select	ENSP00000374490.6:n.1452+1_1452+2delinsGT
ENST00000389840.6:c.1452+1_1452+2delinsGT	ENSP00000374490.6:n.1452+1_1452+2delinsGT
ENST00000585328.5:c.1452+1_1452+2delinsGT	ENSP00000465516.1:n.1452+1_1452+2delinsGT
ENST00000589793.1:n.664+1_664+2delinsGT
NM_173628.3:c.1452+1_1452+2delinsGT	NP_775899.3:n.1452+1_1452+2delinsGT
XM_011525416.1:c.1452+1_1452+2delinsGT	XP_011523718.1:n.1452+1_1452+2delinsGT
XM_011525417.1:c.1452+1_1452+2delinsGT	XP_011523719.1:n.1452+1_1452+2delinsGT
XR_934583.1:n.1613+1_1613+2delinsGT
XM_011525416.2:c.1452+1_1452+2delinsGT	XP_011523718.1:n.1452+1_1452+2delinsGT
XM_024451013.1:c.1452+1_1452+2delinsGT	XP_024306781.1:n.1452+1_1452+2delinsGT
XM_024451014.1:c.1452+1_1452+2delinsGT	XP_024306782.1:n.1452+1_1452+2delinsGT
XR_002958080.1:n.1615+1_1615+2delinsGT
XR_002958081.1:n.1619+1_1619+2delinsGT
NM_173628.4:c.1452+1_1452+2delinsGT MANE Select	NP_775899.3:n.1452+1_1452+2delinsGT