Canonical Allele Identifier: CA1693538804

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558626_21558628delinsTTA , CM000669.2:g.21558626_21558628delinsTTA	GRCh38
NC_000007.13:g.21598244_21598246delinsTTA , CM000669.1:g.21598244_21598246delinsTTA	GRCh37
NC_000007.12:g.21564769_21564771delinsTTA	NCBI36
NG_012886.2:g.20412_20414delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-176_496-174delinsTTA MANE Select	ENSP00000475939.1:n.496-176_496-174delinsTTA
ENST00000328843.10:c.496-176_496-174delinsTTA	ENSP00000330671.7:n.496-176_496-174delinsTTA
ENST00000409508.7:c.496-176_496-174delinsTTA	ENSP00000475939.1:n.496-176_496-174delinsTTA
ENST00000620169.4:c.496-176_496-174delinsTTA	ENSP00000481693.1:n.496-176_496-174delinsTTA
NM_001277115.1:c.496-176_496-174delinsTTA	NP_001264044.1:n.496-176_496-174delinsTTA
NM_001277115.2:c.496-176_496-174delinsTTA MANE Select	NP_001264044.1:n.496-176_496-174delinsTTA