Canonical Allele Identifier: CA4182236

Gene: DNAH11

Linked Data

• ClinVar Variation Id: 359671
• ClinVar RCV Id: RCV000281061
• dbSNP Id: rs763155183
• ExAC: 7:21840849 A / G
• gnomAD v2: 7-21840849-A-G
• gnomAD v3: 7-21801231-A-G
• gnomAD v4: 7-21801231-A-G
• MyVariant Identifiers: chr7:g.21840849A>G (hg19) ; chr7:g.21801231A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21801231A>G , CM000669.2:g.21801231A>G	GRCh38
NC_000007.13:g.21840849A>G , CM000669.1:g.21840849A>G	GRCh37
NC_000007.12:g.21807374A>G	NCBI36
NG_012886.2:g.263017A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.10121A>G MANE Select	ENSP00000475939.1:p.Lys3374Arg
ENST00000328843.10:c.10142A>G	ENSP00000330671.7:p.Lys3381Arg
ENST00000409508.7:c.10121A>G	ENSP00000475939.1:p.Lys3374Arg
ENST00000620169.4:c.10142A>G	ENSP00000481693.1:p.Lys3381Arg
NM_001277115.1:c.10121A>G	NP_001264044.1:p.Lys3374Arg
NM_001277115.2:c.10121A>G MANE Select	NP_001264044.1:p.Lys3374Arg