Canonical Allele Identifier: CA572917814

Gene: DNAH11

Linked Data

• dbSNP Id: rs1583534849
• gnomAD v2: 7-21658885-G-GGGAAAAAAAGT
• MyVariant Identifiers: chr7:g.21658885_21658886insGGAAAAAAAGT (hg19) ; chr7:g.21619267_21619268insGGAAAAAAAGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21619267_21619268insGGAAAAAAAGT , CM000669.2:g.21619267_21619268insGGAAAAAAAGT	GRCh38
NC_000007.13:g.21658885_21658886insGGAAAAAAAGT , CM000669.1:g.21658885_21658886insGGAAAAAAAGT	GRCh37
NC_000007.12:g.21625410_21625411insGGAAAAAAAGT	NCBI36
NG_012886.2:g.81053_81054insGGAAAAAAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.4377+45_4377+46insGGAAAAAAAGT MANE Select	ENSP00000475939.1:n.4377+45_4377+46insGGAAAAAAAGT
ENST00000328843.10:c.4392+45_4392+46insGGAAAAAAAGT	ENSP00000330671.7:n.4392+45_4392+46insGGAAAAAAAGT
ENST00000409508.7:c.4377+45_4377+46insGGAAAAAAAGT	ENSP00000475939.1:n.4377+45_4377+46insGGAAAAAAAGT
ENST00000465593.1:n.403+45_403+46insGGAAAAAAAGT
ENST00000620169.4:c.4392+45_4392+46insGGAAAAAAAGT	ENSP00000481693.1:n.4392+45_4392+46insGGAAAAAAAGT
NM_001277115.1:c.4377+45_4377+46insGGAAAAAAAGT	NP_001264044.1:n.4377+45_4377+46insGGAAAAAAAGT
NM_001277115.2:c.4377+45_4377+46insGGAAAAAAAGT MANE Select	NP_001264044.1:n.4377+45_4377+46insGGAAAAAAAGT