Canonical Allele Identifier: CA1693578806

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21599700_21599701delinsTC , CM000669.2:g.21599700_21599701delinsTC	GRCh38
NC_000007.13:g.21639318_21639319delinsTC , CM000669.1:g.21639318_21639319delinsTC	GRCh37
NC_000007.12:g.21605843_21605844delinsTC	NCBI36
NG_012886.2:g.61486_61487delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.2668-87_2668-86delinsTC MANE Select	ENSP00000475939.1:n.2668-87_2668-86delinsTC
ENST00000328843.10:c.2668-87_2668-86delinsTC	ENSP00000330671.7:n.2668-87_2668-86delinsTC
ENST00000409508.7:c.2668-87_2668-86delinsTC	ENSP00000475939.1:n.2668-87_2668-86delinsTC
ENST00000620169.4:c.2668-87_2668-86delinsTC	ENSP00000481693.1:n.2668-87_2668-86delinsTC
NM_001277115.1:c.2668-87_2668-86delinsTC	NP_001264044.1:n.2668-87_2668-86delinsTC
NM_001277115.2:c.2668-87_2668-86delinsTC MANE Select	NP_001264044.1:n.2668-87_2668-86delinsTC