Canonical Allele Identifier: CA2681979569

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21600200-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21600202_21600203del , CM000669.2:g.21600202_21600203del	GRCh38
NC_000007.13:g.21639820_21639821del , CM000669.1:g.21639820_21639821del	GRCh37
NC_000007.12:g.21606345_21606346del	NCBI36
NG_012886.2:g.61988_61989del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.3000+83_3000+84del MANE Select	ENSP00000475939.1:n.3000+83_3000+84del
ENST00000328843.10:c.3000+83_3000+84del	ENSP00000330671.7:n.3000+83_3000+84del
ENST00000409508.7:c.3000+83_3000+84del	ENSP00000475939.1:n.3000+83_3000+84del
ENST00000620169.4:c.3000+83_3000+84del	ENSP00000481693.1:n.3000+83_3000+84del
NM_001277115.1:c.3000+83_3000+84del	NP_001264044.1:n.3000+83_3000+84del
NM_001277115.2:c.3000+83_3000+84del MANE Select	NP_001264044.1:n.3000+83_3000+84del