Canonical Allele Identifier: CA2681987123

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21748843-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21748843A>G , CM000669.2:g.21748843A>G	GRCh38
NC_000007.13:g.21788461A>G , CM000669.1:g.21788461A>G	GRCh37
NC_000007.12:g.21754986A>G	NCBI36
NG_012886.2:g.210629A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.8673+101A>G MANE Select	ENSP00000475939.1:n.8673+101A>G
ENST00000328843.10:c.8694+101A>G	ENSP00000330671.7:n.8694+101A>G
ENST00000409508.7:c.8673+101A>G	ENSP00000475939.1:n.8673+101A>G
ENST00000620169.4:c.8694+101A>G	ENSP00000481693.1:n.8694+101A>G
NM_001277115.1:c.8673+101A>G	NP_001264044.1:n.8673+101A>G
NM_001277115.2:c.8673+101A>G MANE Select	NP_001264044.1:n.8673+101A>G