Canonical Allele Identifier: CA836691216

Gene: DNAH11

Linked Data

• dbSNP Id: rs367971326
• gnomAD v3: 7-21881133-A-AT
• gnomAD v4: 7-21881133-A-AT
• MyVariant Identifiers: chr7:g.21920751_21920752insT (hg19) ; chr7:g.21881133_21881134insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21881133_21881134insT , CM000669.2:g.21881133_21881134insT	GRCh38
NC_000007.13:g.21920751_21920752insT , CM000669.1:g.21920751_21920752insT	GRCh37
NC_000007.12:g.21887276_21887277insT	NCBI36
NG_012886.2:g.342919_342920insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.12387+240_12387+241insT MANE Select	ENSP00000475939.1:n.12387+240_12387+241insT
ENST00000328843.10:c.12408+240_12408+241insT	ENSP00000330671.7:n.12408+240_12408+241insT
ENST00000409508.7:c.12387+240_12387+241insT	ENSP00000475939.1:n.12387+240_12387+241insT
ENST00000620169.4:c.12408+240_12408+241insT	ENSP00000481693.1:n.12408+240_12408+241insT
NM_001277115.1:c.12387+240_12387+241insT	NP_001264044.1:n.12387+240_12387+241insT
NM_001277115.2:c.12387+240_12387+241insT MANE Select	NP_001264044.1:n.12387+240_12387+241insT