Canonical Allele Identifier: CA1693538901

Gene: DNAH11

Linked Data

• dbSNP Id: rs1783318279

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558693_21558694insAGA , CM000669.2:g.21558693_21558694insAGA	GRCh38
NC_000007.13:g.21598311_21598312insAGA , CM000669.1:g.21598311_21598312insAGA	GRCh37
NC_000007.12:g.21564836_21564837insAGA	NCBI36
NG_012886.2:g.20479_20480insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-109_496-108insAGA MANE Select	ENSP00000475939.1:n.496-109_496-108insAGA
ENST00000328843.10:c.496-109_496-108insAGA	ENSP00000330671.7:n.496-109_496-108insAGA
ENST00000409508.7:c.496-109_496-108insAGA	ENSP00000475939.1:n.496-109_496-108insAGA
ENST00000620169.4:c.496-109_496-108insAGA	ENSP00000481693.1:n.496-109_496-108insAGA
NM_001277115.1:c.496-109_496-108insAGA	NP_001264044.1:n.496-109_496-108insAGA
NM_001277115.2:c.496-109_496-108insAGA MANE Select	NP_001264044.1:n.496-109_496-108insAGA