Canonical Allele Identifier: CA1693537966
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21543345_21543346delinsGA , CM000669.2:g.21543345_21543346delinsGA GRCh38
NC_000007.13:g.21582963_21582964delinsGA , CM000669.1:g.21582963_21582964delinsGA GRCh37
NC_000007.12:g.21549488_21549489delinsGA NCBI36
NG_012886.2:g.5131_5132delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.100_101delinsGA MANE Select ENSP00000475939.1:p.Glu34=
ENST00000328843.10:c.100_101delinsGA ENSP00000330671.7:p.Glu34=
ENST00000409508.7:c.100_101delinsGA ENSP00000475939.1:p.Glu34=
ENST00000620169.4:c.100_101delinsGA ENSP00000481693.1:p.Glu34=
NM_001277115.1:c.100_101delinsGA NP_001264044.1:p.Glu34=
NM_001277115.2:c.100_101delinsGA MANE Select NP_001264044.1:p.Glu34=