Canonical Allele Identifier: CA2774680442

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21816848_21816849insACA , CM000669.2:g.21816848_21816849insACA	GRCh38
NC_000007.13:g.21856466_21856467insACA , CM000669.1:g.21856466_21856467insACA	GRCh37
NC_000007.12:g.21822991_21822992insACA	NCBI36
NG_012886.2:g.278634_278635insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.10568+146_10568+147insACA MANE Select	ENSP00000475939.1:n.10568+146_10568+147insACA
ENST00000328843.10:c.10589+146_10589+147insACA	ENSP00000330671.7:n.10589+146_10589+147insACA
ENST00000409508.7:c.10568+146_10568+147insACA	ENSP00000475939.1:n.10568+146_10568+147insACA
ENST00000620169.4:c.10589+146_10589+147insACA	ENSP00000481693.1:n.10589+146_10589+147insACA
NM_001277115.1:c.10568+146_10568+147insACA	NP_001264044.1:n.10568+146_10568+147insACA
NM_001277115.2:c.10568+146_10568+147insACA MANE Select	NP_001264044.1:n.10568+146_10568+147insACA