Canonical Allele Identifier: CA1693665976

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21816295_21816296delinsAT , CM000669.2:g.21816295_21816296delinsAT	GRCh38
NC_000007.13:g.21855913_21855914delinsAT , CM000669.1:g.21855913_21855914delinsAT	GRCh37
NC_000007.12:g.21822438_21822439delinsAT	NCBI36
NG_012886.2:g.278081_278082delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.10333-172_10333-171delinsAT MANE Select	ENSP00000475939.1:n.10333-172_10333-171delinsAT
ENST00000328843.10:c.10354-172_10354-171delinsAT	ENSP00000330671.7:n.10354-172_10354-171delinsAT
ENST00000409508.7:c.10333-172_10333-171delinsAT	ENSP00000475939.1:n.10333-172_10333-171delinsAT
ENST00000620169.4:c.10354-172_10354-171delinsAT	ENSP00000481693.1:n.10354-172_10354-171delinsAT
NM_001277115.1:c.10333-172_10333-171delinsAT	NP_001264044.1:n.10333-172_10333-171delinsAT
NM_001277115.2:c.10333-172_10333-171delinsAT MANE Select	NP_001264044.1:n.10333-172_10333-171delinsAT