Canonical Allele Identifier: CA651450701

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21816786-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21816786A>G , CM000669.2:g.21816786A>G	GRCh38
NC_000007.13:g.21856404A>G , CM000669.1:g.21856404A>G	GRCh37
NC_000007.12:g.21822929A>G	NCBI36
NG_012886.2:g.278572A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.10568+84A>G MANE Select	ENSP00000475939.1:n.10568+84A>G
ENST00000328843.10:c.10589+84A>G	ENSP00000330671.7:n.10589+84A>G
ENST00000409508.7:c.10568+84A>G	ENSP00000475939.1:n.10568+84A>G
ENST00000620169.4:c.10589+84A>G	ENSP00000481693.1:n.10589+84A>G
NM_001277115.1:c.10568+84A>G	NP_001264044.1:n.10568+84A>G
NM_001277115.2:c.10568+84A>G MANE Select	NP_001264044.1:n.10568+84A>G