Canonical Allele Identifier: CA4178727

Gene: DNAH11

Linked Data

• ClinVar Variation Id: 454697
• ClinVar RCV Id: RCV000551357
• dbSNP Id: rs765936290
• ExAC: 7:21598560 A / G
• gnomAD v2: 7-21598560-A-G
• gnomAD v3: 7-21558942-A-G
• gnomAD v4: 7-21558942-A-G
• MyVariant Identifiers: chr7:g.21598560A>G (hg19) ; chr7:g.21558942A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558942A>G , CM000669.2:g.21558942A>G	GRCh38
NC_000007.13:g.21598560A>G , CM000669.1:g.21598560A>G	GRCh37
NC_000007.12:g.21565085A>G	NCBI36
NG_012886.2:g.20728A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.636A>G MANE Select	ENSP00000475939.1:p.Leu212=
ENST00000328843.10:c.636A>G	ENSP00000330671.7:p.Leu212=
ENST00000409508.7:c.636A>G	ENSP00000475939.1:p.Leu212=
ENST00000620169.4:c.636A>G	ENSP00000481693.1:p.Leu212=
NM_001277115.1:c.636A>G	NP_001264044.1:p.Leu212=
NM_001277115.2:c.636A>G MANE Select	NP_001264044.1:p.Leu212=