Canonical Allele Identifier: CA1693571259

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21618960_21618961delinsTC , CM000669.2:g.21618960_21618961delinsTC	GRCh38
NC_000007.13:g.21658578_21658579delinsTC , CM000669.1:g.21658578_21658579delinsTC	GRCh37
NC_000007.12:g.21625103_21625104delinsTC	NCBI36
NG_012886.2:g.80746_80747delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.4255-140_4255-139delinsTC MANE Select	ENSP00000475939.1:n.4255-140_4255-139delinsTC
ENST00000328843.10:c.4270-140_4270-139delinsTC	ENSP00000330671.7:n.4270-140_4270-139delinsTC
ENST00000409508.7:c.4255-140_4255-139delinsTC	ENSP00000475939.1:n.4255-140_4255-139delinsTC
ENST00000465593.1:n.281-140_281-139delinsTC
ENST00000620169.4:c.4270-140_4270-139delinsTC	ENSP00000481693.1:n.4270-140_4270-139delinsTC
NM_001277115.1:c.4255-140_4255-139delinsTC	NP_001264044.1:n.4255-140_4255-139delinsTC
NM_001277115.2:c.4255-140_4255-139delinsTC MANE Select	NP_001264044.1:n.4255-140_4255-139delinsTC