Canonical Allele Identifier: CA1693627102

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21705745_21705747delinsAAT , CM000669.2:g.21705745_21705747delinsAAT	GRCh38
NC_000007.13:g.21745363_21745365delinsAAT , CM000669.1:g.21745363_21745365delinsAAT	GRCh37
NC_000007.12:g.21711888_21711890delinsAAT	NCBI36
NG_012886.2:g.167531_167533delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.6546+208_6546+210delinsAAT MANE Select	ENSP00000475939.1:n.6546+208_6546+210delinsAAT
ENST00000328843.10:c.6567+208_6567+210delinsAAT	ENSP00000330671.7:n.6567+208_6567+210delinsAAT
ENST00000409508.7:c.6546+208_6546+210delinsAAT	ENSP00000475939.1:n.6546+208_6546+210delinsAAT
ENST00000620169.4:c.6567+208_6567+210delinsAAT	ENSP00000481693.1:n.6567+208_6567+210delinsAAT
NM_001277115.1:c.6546+208_6546+210delinsAAT	NP_001264044.1:n.6546+208_6546+210delinsAAT
NM_001277115.2:c.6546+208_6546+210delinsAAT MANE Select	NP_001264044.1:n.6546+208_6546+210delinsAAT