Canonical Allele Identifier: CA155074739

Gene: DNAH11

Linked Data

• dbSNP Id: rs757562664
• gnomAD v2: 7-21598760-A-G
• gnomAD v3: 7-21559142-A-G
• gnomAD v4: 7-21559142-A-G
• MyVariant Identifiers: chr7:g.21598760A>G (hg19) ; chr7:g.21559142A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21559142A>G , CM000669.2:g.21559142A>G	GRCh38
NC_000007.13:g.21598760A>G , CM000669.1:g.21598760A>G	GRCh37
NC_000007.12:g.21565285A>G	NCBI36
NG_012886.2:g.20928A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.692+144A>G MANE Select	ENSP00000475939.1:n.692+144A>G
ENST00000328843.10:c.692+144A>G	ENSP00000330671.7:n.692+144A>G
ENST00000409508.7:c.692+144A>G	ENSP00000475939.1:n.692+144A>G
ENST00000620169.4:c.692+144A>G	ENSP00000481693.1:n.692+144A>G
NM_001277115.1:c.692+144A>G	NP_001264044.1:n.692+144A>G
NM_001277115.2:c.692+144A>G MANE Select	NP_001264044.1:n.692+144A>G