Canonical Allele Identifier: CA4182375

Gene: DNAH11

Linked Data

• ClinVar Variation Id: 2794073
• ClinVar RCV Id: RCV003647362
• dbSNP Id: rs745461419
• ExAC: 7:21856249 G / A
• gnomAD v2: 7-21856249-G-A
• gnomAD v3: 7-21816631-G-A
• gnomAD v4: 7-21816631-G-A
• MyVariant Identifiers: chr7:g.21856249G>A (hg19) ; chr7:g.21816631G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21816631G>A , CM000669.2:g.21816631G>A	GRCh38
NC_000007.13:g.21856249G>A , CM000669.1:g.21856249G>A	GRCh37
NC_000007.12:g.21822774G>A	NCBI36
NG_012886.2:g.278417G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.10497G>A MANE Select	ENSP00000475939.1:p.Gln3499=
ENST00000328843.10:c.10518G>A	ENSP00000330671.7:p.Gln3506=
ENST00000409508.7:c.10497G>A	ENSP00000475939.1:p.Gln3499=
ENST00000620169.4:c.10518G>A	ENSP00000481693.1:p.Gln3506=
NM_001277115.1:c.10497G>A	NP_001264044.1:p.Gln3499=
NM_001277115.2:c.10497G>A MANE Select	NP_001264044.1:p.Gln3499=