Canonical Allele Identifier: CA155122463

Gene: DNAH11

Linked Data

• dbSNP Id: rs35467098
• MyVariant Identifiers: chr7:g.21856648_21856649insT (hg19) ; chr7:g.21817030_21817031insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21817030_21817031insT , CM000669.2:g.21817030_21817031insT	GRCh38
NC_000007.13:g.21856648_21856649insT , CM000669.1:g.21856648_21856649insT	GRCh37
NC_000007.12:g.21823173_21823174insT	NCBI36
NG_012886.2:g.278816_278817insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.10568+328_10568+329insT MANE Select	ENSP00000475939.1:n.10568+328_10568+329insT
ENST00000328843.10:c.10589+328_10589+329insT	ENSP00000330671.7:n.10589+328_10589+329insT
ENST00000409508.7:c.10568+328_10568+329insT	ENSP00000475939.1:n.10568+328_10568+329insT
ENST00000620169.4:c.10589+328_10589+329insT	ENSP00000481693.1:n.10589+328_10589+329insT
NM_001277115.1:c.10568+328_10568+329insT	NP_001264044.1:n.10568+328_10568+329insT
NM_001277115.2:c.10568+328_10568+329insT MANE Select	NP_001264044.1:n.10568+328_10568+329insT