Canonical Allele Identifier: CA836624889

Gene: DNAH11

Linked Data

• dbSNP Id: rs1289909219
• gnomAD v3: 7-21618943-AG-A
• gnomAD v4: 7-21618943-AG-A
• MyVariant Identifiers: chr7:g.21658562del (hg19) ; chr7:g.21618944del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21618945del , CM000669.2:g.21618945del	GRCh38
NC_000007.13:g.21658563del , CM000669.1:g.21658563del	GRCh37
NC_000007.12:g.21625088del	NCBI36
NG_012886.2:g.80731del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.4255-155del MANE Select	ENSP00000475939.1:n.4255-155del
ENST00000328843.10:c.4270-155del	ENSP00000330671.7:n.4270-155del
ENST00000409508.7:c.4255-155del	ENSP00000475939.1:n.4255-155del
ENST00000465593.1:n.281-155del
ENST00000620169.4:c.4270-155del	ENSP00000481693.1:n.4270-155del
NM_001277115.1:c.4255-155del	NP_001264044.1:n.4255-155del
NM_001277115.2:c.4255-155del MANE Select	NP_001264044.1:n.4255-155del