Canonical Allele Identifier: CA1693538751

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558578_21558579delinsTG , CM000669.2:g.21558578_21558579delinsTG	GRCh38
NC_000007.13:g.21598196_21598197delinsTG , CM000669.1:g.21598196_21598197delinsTG	GRCh37
NC_000007.12:g.21564721_21564722delinsTG	NCBI36
NG_012886.2:g.20364_20365delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-224_496-223delinsTG MANE Select	ENSP00000475939.1:n.496-224_496-223delinsTG
ENST00000328843.10:c.496-224_496-223delinsTG	ENSP00000330671.7:n.496-224_496-223delinsTG
ENST00000409508.7:c.496-224_496-223delinsTG	ENSP00000475939.1:n.496-224_496-223delinsTG
ENST00000620169.4:c.496-224_496-223delinsTG	ENSP00000481693.1:n.496-224_496-223delinsTG
NM_001277115.1:c.496-224_496-223delinsTG	NP_001264044.1:n.496-224_496-223delinsTG
NM_001277115.2:c.496-224_496-223delinsTG MANE Select	NP_001264044.1:n.496-224_496-223delinsTG