Canonical Allele Identifier: CA1693538814

Gene: DNAH11

Linked Data

• dbSNP Id: rs1783315537

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558628_21558629del , CM000669.2:g.21558628_21558629del	GRCh38
NC_000007.13:g.21598246_21598247del , CM000669.1:g.21598246_21598247del	GRCh37
NC_000007.12:g.21564771_21564772del	NCBI36
NG_012886.2:g.20414_20415del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-174_496-173del MANE Select	ENSP00000475939.1:n.496-174_496-173del
ENST00000328843.10:c.496-174_496-173del	ENSP00000330671.7:n.496-174_496-173del
ENST00000409508.7:c.496-174_496-173del	ENSP00000475939.1:n.496-174_496-173del
ENST00000620169.4:c.496-174_496-173del	ENSP00000481693.1:n.496-174_496-173del
NM_001277115.1:c.496-174_496-173del	NP_001264044.1:n.496-174_496-173del
NM_001277115.2:c.496-174_496-173del MANE Select	NP_001264044.1:n.496-174_496-173del