Canonical Allele Identifier: CA1693571420

Gene: DNAH11

Linked Data

• dbSNP Id: rs1785916032

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21619078dup , CM000669.2:g.21619078dup	GRCh38
NC_000007.13:g.21658696dup , CM000669.1:g.21658696dup	GRCh37
NC_000007.12:g.21625221dup	NCBI36
NG_012886.2:g.80864dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.4255-22dup MANE Select	ENSP00000475939.1:n.4255-22dup
ENST00000328843.10:c.4270-22dup	ENSP00000330671.7:n.4270-22dup
ENST00000409508.7:c.4255-22dup	ENSP00000475939.1:n.4255-22dup
ENST00000465593.1:n.281-22dup
ENST00000620169.4:c.4270-22dup	ENSP00000481693.1:n.4270-22dup
NM_001277115.1:c.4255-22dup	NP_001264044.1:n.4255-22dup
NM_001277115.2:c.4255-22dup MANE Select	NP_001264044.1:n.4255-22dup