Canonical Allele Identifier: CA4179655
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 454670
dbSNP Id: rs370436662
gnomAD v2: 7-21641082-A-G
gnomAD v3: 7-21601464-A-G
gnomAD v4: 7-21601464-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21601464A>G , CM000669.2:g.21601464A>G GRCh38
NC_000007.13:g.21641082A>G , CM000669.1:g.21641082A>G GRCh37
NC_000007.12:g.21607607A>G NCBI36
NG_012886.2:g.63250A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.3494A>G MANE Select ENSP00000475939.1:p.Asp1165Gly
ENST00000328843.10:c.3494A>G ENSP00000330671.7:p.Asp1165Gly
ENST00000409508.7:c.3494A>G ENSP00000475939.1:p.Asp1165Gly
ENST00000620169.4:c.3494A>G ENSP00000481693.1:p.Asp1165Gly
NM_001277115.1:c.3494A>G NP_001264044.1:p.Asp1165Gly
NM_001277115.2:c.3494A>G MANE Select NP_001264044.1:p.Asp1165Gly