Canonical Allele Identifier: CA4182606

Gene: DNAH11

Linked Data

• dbSNP Id: rs779655850
• ExAC: 7:21893912 T / A
• gnomAD v2: 7-21893912-T-A
• gnomAD v4: 7-21854294-T-A
• MyVariant Identifiers: chr7:g.21893912T>A (hg19) ; chr7:g.21854294T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21854294T>A , CM000669.2:g.21854294T>A	GRCh38
NC_000007.13:g.21893912T>A , CM000669.1:g.21893912T>A	GRCh37
NC_000007.12:g.21860437T>A	NCBI36
NG_012886.2:g.316080T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.11062-21T>A MANE Select	ENSP00000475939.1:n.11062-21T>A
ENST00000328843.10:c.11083-21T>A	ENSP00000330671.7:n.11083-21T>A
ENST00000409508.7:c.11062-21T>A	ENSP00000475939.1:n.11062-21T>A
ENST00000421290.1:n.245-21T>A
ENST00000607413.5:n.325-21T>A
ENST00000620169.4:c.11083-21T>A	ENSP00000481693.1:n.11083-21T>A
NM_001277115.1:c.11062-21T>A	NP_001264044.1:n.11062-21T>A
NM_001277115.2:c.11062-21T>A MANE Select	NP_001264044.1:n.11062-21T>A