Canonical Allele Identifier: CA2681979374

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21599698-CTTCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21599701_21599705del , CM000669.2:g.21599701_21599705del	GRCh38
NC_000007.13:g.21639319_21639323del , CM000669.1:g.21639319_21639323del	GRCh37
NC_000007.12:g.21605844_21605848del	NCBI36
NG_012886.2:g.61487_61491del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.2668-86_2668-82del MANE Select	ENSP00000475939.1:n.2668-86_2668-82del
ENST00000328843.10:c.2668-86_2668-82del	ENSP00000330671.7:n.2668-86_2668-82del
ENST00000409508.7:c.2668-86_2668-82del	ENSP00000475939.1:n.2668-86_2668-82del
ENST00000620169.4:c.2668-86_2668-82del	ENSP00000481693.1:n.2668-86_2668-82del
NM_001277115.1:c.2668-86_2668-82del	NP_001264044.1:n.2668-86_2668-82del
NM_001277115.2:c.2668-86_2668-82del MANE Select	NP_001264044.1:n.2668-86_2668-82del