Canonical Allele Identifier: CA2681992386

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21881031-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21881035_21881036del , CM000669.2:g.21881035_21881036del	GRCh38
NC_000007.13:g.21920653_21920654del , CM000669.1:g.21920653_21920654del	GRCh37
NC_000007.12:g.21887178_21887179del	NCBI36
NG_012886.2:g.342821_342822del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.12387+142_12387+143del MANE Select	ENSP00000475939.1:n.12387+142_12387+143del
ENST00000328843.10:c.12408+142_12408+143del	ENSP00000330671.7:n.12408+142_12408+143del
ENST00000409508.7:c.12387+142_12387+143del	ENSP00000475939.1:n.12387+142_12387+143del
ENST00000620169.4:c.12408+142_12408+143del	ENSP00000481693.1:n.12408+142_12408+143del
NM_001277115.1:c.12387+142_12387+143del	NP_001264044.1:n.12387+142_12387+143del
NM_001277115.2:c.12387+142_12387+143del MANE Select	NP_001264044.1:n.12387+142_12387+143del