Canonical Allele Identifier: CA2681976804

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21559142-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21559144_21559145del , CM000669.2:g.21559144_21559145del	GRCh38
NC_000007.13:g.21598762_21598763del , CM000669.1:g.21598762_21598763del	GRCh37
NC_000007.12:g.21565287_21565288del	NCBI36
NG_012886.2:g.20930_20931del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.692+146_692+147del MANE Select	ENSP00000475939.1:n.692+146_692+147del
ENST00000328843.10:c.692+146_692+147del	ENSP00000330671.7:n.692+146_692+147del
ENST00000409508.7:c.692+146_692+147del	ENSP00000475939.1:n.692+146_692+147del
ENST00000620169.4:c.692+146_692+147del	ENSP00000481693.1:n.692+146_692+147del
NM_001277115.1:c.692+146_692+147del	NP_001264044.1:n.692+146_692+147del
NM_001277115.2:c.692+146_692+147del MANE Select	NP_001264044.1:n.692+146_692+147del