Canonical Allele Identifier: CA2681991210

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21864484-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21864484A>G , CM000669.2:g.21864484A>G	GRCh38
NC_000007.13:g.21904102A>G , CM000669.1:g.21904102A>G	GRCh37
NC_000007.12:g.21870627A>G	NCBI36
NG_012886.2:g.326270A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.11374-51A>G MANE Select	ENSP00000475939.1:n.11374-51A>G
ENST00000328843.10:c.11395-51A>G	ENSP00000330671.7:n.11395-51A>G
ENST00000409508.7:c.11374-51A>G	ENSP00000475939.1:n.11374-51A>G
ENST00000620169.4:c.11395-51A>G	ENSP00000481693.1:n.11395-51A>G
NM_001277115.1:c.11374-51A>G	NP_001264044.1:n.11374-51A>G
NM_001277115.2:c.11374-51A>G MANE Select	NP_001264044.1:n.11374-51A>G