Canonical Allele Identifier: CA2681981424

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21619315-G-GACTCATCTCTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21619316_21619317insCTCATCTCTCCA , CM000669.2:g.21619316_21619317insCTCATCTCTCCA	GRCh38
NC_000007.13:g.21658934_21658935insCTCATCTCTCCA , CM000669.1:g.21658934_21658935insCTCATCTCTCCA	GRCh37
NC_000007.12:g.21625459_21625460insCTCATCTCTCCA	NCBI36
NG_012886.2:g.81102_81103insCTCATCTCTCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.4377+94_4377+95insCTCATCTCTCCA MANE Select	ENSP00000475939.1:n.4377+94_4377+95insCTCATCTCTCCA
ENST00000328843.10:c.4392+94_4392+95insCTCATCTCTCCA	ENSP00000330671.7:n.4392+94_4392+95insCTCATCTCTCCA
ENST00000409508.7:c.4377+94_4377+95insCTCATCTCTCCA	ENSP00000475939.1:n.4377+94_4377+95insCTCATCTCTCCA
ENST00000465593.1:n.403+94_403+95insCTCATCTCTCCA
ENST00000620169.4:c.4392+94_4392+95insCTCATCTCTCCA	ENSP00000481693.1:n.4392+94_4392+95insCTCATCTCTCCA
NM_001277115.1:c.4377+94_4377+95insCTCATCTCTCCA	NP_001264044.1:n.4377+94_4377+95insCTCATCTCTCCA
NM_001277115.2:c.4377+94_4377+95insCTCATCTCTCCA MANE Select	NP_001264044.1:n.4377+94_4377+95insCTCATCTCTCCA