Canonical Allele Identifier: CA1693538989

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558738_21558741delinsCAAG , CM000669.2:g.21558738_21558741delinsCAAG	GRCh38
NC_000007.13:g.21598356_21598359delinsCAAG , CM000669.1:g.21598356_21598359delinsCAAG	GRCh37
NC_000007.12:g.21564881_21564884delinsCAAG	NCBI36
NG_012886.2:g.20524_20527delinsCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-64_496-61delinsCAAG MANE Select	ENSP00000475939.1:n.496-64_496-61delinsCAAG
ENST00000328843.10:c.496-64_496-61delinsCAAG	ENSP00000330671.7:n.496-64_496-61delinsCAAG
ENST00000409508.7:c.496-64_496-61delinsCAAG	ENSP00000475939.1:n.496-64_496-61delinsCAAG
ENST00000620169.4:c.496-64_496-61delinsCAAG	ENSP00000481693.1:n.496-64_496-61delinsCAAG
NM_001277115.1:c.496-64_496-61delinsCAAG	NP_001264044.1:n.496-64_496-61delinsCAAG
NM_001277115.2:c.496-64_496-61delinsCAAG MANE Select	NP_001264044.1:n.496-64_496-61delinsCAAG