Canonical Allele Identifier: CA836622754

Gene: DNAH11

Linked Data

• dbSNP Id: rs1445796403
• gnomAD v3: 7-21664334-T-G
• gnomAD v4: 7-21664334-T-G
• MyVariant Identifiers: chr7:g.21703952T>G (hg19) ; chr7:g.21664334T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21664334T>G , CM000669.2:g.21664334T>G	GRCh38
NC_000007.13:g.21703952T>G , CM000669.1:g.21703952T>G	GRCh37
NC_000007.12:g.21670477T>G	NCBI36
NG_012886.2:g.126120T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.5328+5303T>G MANE Select	ENSP00000475939.1:n.5328+5303T>G
ENST00000328843.10:c.5343+5303T>G	ENSP00000330671.7:n.5343+5303T>G
ENST00000409508.7:c.5328+5303T>G	ENSP00000475939.1:n.5328+5303T>G
ENST00000620169.4:c.5343+5303T>G	ENSP00000481693.1:n.5343+5303T>G
NM_001277115.1:c.5328+5303T>G	NP_001264044.1:n.5328+5303T>G
NM_001277115.2:c.5328+5303T>G MANE Select	NP_001264044.1:n.5328+5303T>G