Canonical Allele Identifier: CA4179480

Gene: DNAH11

Linked Data

• ClinVar Variation Id: 2146688
• ClinVar RCV Id: RCV003067255
• dbSNP Id: rs374576335
• ExAC: 7:21639710 A / G
• gnomAD v2: 7-21639710-A-G
• gnomAD v3: 7-21600092-A-G
• gnomAD v4: 7-21600092-A-G
• MyVariant Identifiers: chr7:g.21639710A>G (hg19) ; chr7:g.21600092A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21600092A>G , CM000669.2:g.21600092A>G	GRCh38
NC_000007.13:g.21639710A>G , CM000669.1:g.21639710A>G	GRCh37
NC_000007.12:g.21606235A>G	NCBI36
NG_012886.2:g.61878A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.2973A>G MANE Select	ENSP00000475939.1:p.Ala991=
ENST00000328843.10:c.2973A>G	ENSP00000330671.7:p.Ala991=
ENST00000409508.7:c.2973A>G	ENSP00000475939.1:p.Ala991=
ENST00000620169.4:c.2973A>G	ENSP00000481693.1:p.Ala991=
NM_001277115.1:c.2973A>G	NP_001264044.1:p.Ala991=
NM_001277115.2:c.2973A>G MANE Select	NP_001264044.1:p.Ala991=