Canonical Allele Identifier: CA2681976583

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21558673-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558675_21558676del , CM000669.2:g.21558675_21558676del	GRCh38
NC_000007.13:g.21598293_21598294del , CM000669.1:g.21598293_21598294del	GRCh37
NC_000007.12:g.21564818_21564819del	NCBI36
NG_012886.2:g.20461_20462del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-127_496-126del MANE Select	ENSP00000475939.1:n.496-127_496-126del
ENST00000328843.10:c.496-127_496-126del	ENSP00000330671.7:n.496-127_496-126del
ENST00000409508.7:c.496-127_496-126del	ENSP00000475939.1:n.496-127_496-126del
ENST00000620169.4:c.496-127_496-126del	ENSP00000481693.1:n.496-127_496-126del
NM_001277115.1:c.496-127_496-126del	NP_001264044.1:n.496-127_496-126del
NM_001277115.2:c.496-127_496-126del MANE Select	NP_001264044.1:n.496-127_496-126del