Canonical Allele Identifier: CA175710

Gene: DNAH11

Linked Data

• ClinVar Variation Id: 163099
• ClinVar RCV Id: RCV000150430 ; RCV000231791 ; RCV000724631
• dbSNP Id: rs191266255
• ExAC: 7:21629018 A / G
• gnomAD v2: 7-21629018-A-G
• gnomAD v3: 7-21589400-A-G
• gnomAD v4: 7-21589400-A-G
• MyVariant Identifiers: chr7:g.21629018A>G (hg19) ; chr7:g.21589400A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21589400A>G , CM000669.2:g.21589400A>G	GRCh38
NC_000007.13:g.21629018A>G , CM000669.1:g.21629018A>G	GRCh37
NC_000007.12:g.21595543A>G	NCBI36
NG_012886.2:g.51186A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.2166A>G MANE Select	ENSP00000475939.1:p.Pro722=
ENST00000328843.10:c.2166A>G	ENSP00000330671.7:p.Pro722=
ENST00000409508.7:c.2166A>G	ENSP00000475939.1:p.Pro722=
ENST00000620169.4:c.2166A>G	ENSP00000481693.1:p.Pro722=
NM_001277115.1:c.2166A>G	NP_001264044.1:p.Pro722=
NM_001277115.2:c.2166A>G MANE Select	NP_001264044.1:p.Pro722=