Canonical Allele Identifier: CA2681976622

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21558698-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558700_21558701dup , CM000669.2:g.21558700_21558701dup	GRCh38
NC_000007.13:g.21598318_21598319dup , CM000669.1:g.21598318_21598319dup	GRCh37
NC_000007.12:g.21564843_21564844dup	NCBI36
NG_012886.2:g.20486_20487dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-102_496-101dup MANE Select	ENSP00000475939.1:n.496-102_496-101dup
ENST00000328843.10:c.496-102_496-101dup	ENSP00000330671.7:n.496-102_496-101dup
ENST00000409508.7:c.496-102_496-101dup	ENSP00000475939.1:n.496-102_496-101dup
ENST00000620169.4:c.496-102_496-101dup	ENSP00000481693.1:n.496-102_496-101dup
NM_001277115.1:c.496-102_496-101dup	NP_001264044.1:n.496-102_496-101dup
NM_001277115.2:c.496-102_496-101dup MANE Select	NP_001264044.1:n.496-102_496-101dup