Canonical Allele Identifier: CA2681989679

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21816788-C-CCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21816788_21816789insCTG , CM000669.2:g.21816788_21816789insCTG	GRCh38
NC_000007.13:g.21856406_21856407insCTG , CM000669.1:g.21856406_21856407insCTG	GRCh37
NC_000007.12:g.21822931_21822932insCTG	NCBI36
NG_012886.2:g.278574_278575insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.10568+86_10568+87insCTG MANE Select	ENSP00000475939.1:n.10568+86_10568+87insCTG
ENST00000328843.10:c.10589+86_10589+87insCTG	ENSP00000330671.7:n.10589+86_10589+87insCTG
ENST00000409508.7:c.10568+86_10568+87insCTG	ENSP00000475939.1:n.10568+86_10568+87insCTG
ENST00000620169.4:c.10589+86_10589+87insCTG	ENSP00000481693.1:n.10589+86_10589+87insCTG
NM_001277115.1:c.10568+86_10568+87insCTG	NP_001264044.1:n.10568+86_10568+87insCTG
NM_001277115.2:c.10568+86_10568+87insCTG MANE Select	NP_001264044.1:n.10568+86_10568+87insCTG