Canonical Allele Identifier: CA1693578774
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21599654_21599660delinsCTTAGTA , CM000669.2:g.21599654_21599660delinsCTTAGTA GRCh38
NC_000007.13:g.21639272_21639278delinsCTTAGTA , CM000669.1:g.21639272_21639278delinsCTTAGTA GRCh37
NC_000007.12:g.21605797_21605803delinsCTTAGTA NCBI36
NG_012886.2:g.61440_61446delinsCTTAGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.2668-133_2668-127delinsCTTAGTA MANE Select ENSP00000475939.1:n.2668-133_2668-127delinsCTTAGTA
ENST00000328843.10:c.2668-133_2668-127delinsCTTAGTA ENSP00000330671.7:n.2668-133_2668-127delinsCTTAGTA
ENST00000409508.7:c.2668-133_2668-127delinsCTTAGTA ENSP00000475939.1:n.2668-133_2668-127delinsCTTAGTA
ENST00000620169.4:c.2668-133_2668-127delinsCTTAGTA ENSP00000481693.1:n.2668-133_2668-127delinsCTTAGTA
NM_001277115.1:c.2668-133_2668-127delinsCTTAGTA NP_001264044.1:n.2668-133_2668-127delinsCTTAGTA
NM_001277115.2:c.2668-133_2668-127delinsCTTAGTA MANE Select NP_001264044.1:n.2668-133_2668-127delinsCTTAGTA