Canonical Allele Identifier: CA836666478

Gene: DNAH11

Linked Data

• dbSNP Id: rs1335127458
• gnomAD v3: 7-21816343-T-G
• gnomAD v4: 7-21816343-T-G
• MyVariant Identifiers: chr7:g.21855961T>G (hg19) ; chr7:g.21816343T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21816343T>G , CM000669.2:g.21816343T>G	GRCh38
NC_000007.13:g.21855961T>G , CM000669.1:g.21855961T>G	GRCh37
NC_000007.12:g.21822486T>G	NCBI36
NG_012886.2:g.278129T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.10333-124T>G MANE Select	ENSP00000475939.1:n.10333-124T>G
ENST00000328843.10:c.10354-124T>G	ENSP00000330671.7:n.10354-124T>G
ENST00000409508.7:c.10333-124T>G	ENSP00000475939.1:n.10333-124T>G
ENST00000620169.4:c.10354-124T>G	ENSP00000481693.1:n.10354-124T>G
NM_001277115.1:c.10333-124T>G	NP_001264044.1:n.10333-124T>G
NM_001277115.2:c.10333-124T>G MANE Select	NP_001264044.1:n.10333-124T>G