Canonical Allele Identifier: CA2681976796

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21559140-ATAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21559142_21559144del , CM000669.2:g.21559142_21559144del	GRCh38
NC_000007.13:g.21598760_21598762del , CM000669.1:g.21598760_21598762del	GRCh37
NC_000007.12:g.21565285_21565287del	NCBI36
NG_012886.2:g.20928_20930del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.692+144_692+146del MANE Select	ENSP00000475939.1:n.692+144_692+146del
ENST00000328843.10:c.692+144_692+146del	ENSP00000330671.7:n.692+144_692+146del
ENST00000409508.7:c.692+144_692+146del	ENSP00000475939.1:n.692+144_692+146del
ENST00000620169.4:c.692+144_692+146del	ENSP00000481693.1:n.692+144_692+146del
NM_001277115.1:c.692+144_692+146del	NP_001264044.1:n.692+144_692+146del
NM_001277115.2:c.692+144_692+146del MANE Select	NP_001264044.1:n.692+144_692+146del