Canonical Allele Identifier: CA1693713168

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21881216_21881217delinsAT , CM000669.2:g.21881216_21881217delinsAT	GRCh38
NC_000007.13:g.21920834_21920835delinsAT , CM000669.1:g.21920834_21920835delinsAT	GRCh37
NC_000007.12:g.21887359_21887360delinsAT	NCBI36
NG_012886.2:g.343002_343003delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.12387+323_12387+324delinsAT MANE Select	ENSP00000475939.1:n.12387+323_12387+324delinsAT
ENST00000328843.10:c.12408+323_12408+324delinsAT	ENSP00000330671.7:n.12408+323_12408+324delinsAT
ENST00000409508.7:c.12387+323_12387+324delinsAT	ENSP00000475939.1:n.12387+323_12387+324delinsAT
ENST00000620169.4:c.12408+323_12408+324delinsAT	ENSP00000481693.1:n.12408+323_12408+324delinsAT
NM_001277115.1:c.12387+323_12387+324delinsAT	NP_001264044.1:n.12387+323_12387+324delinsAT
NM_001277115.2:c.12387+323_12387+324delinsAT MANE Select	NP_001264044.1:n.12387+323_12387+324delinsAT