Canonical Allele Identifier: CA836691234

Gene: DNAH11

Linked Data

• dbSNP Id: rs1255442577
• gnomAD v3: 7-21881216-AT-A
• gnomAD v4: 7-21881216-AT-A
• MyVariant Identifiers: chr7:g.21920835del (hg19) ; chr7:g.21881217del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21881219del , CM000669.2:g.21881219del	GRCh38
NC_000007.13:g.21920837del , CM000669.1:g.21920837del	GRCh37
NC_000007.12:g.21887362del	NCBI36
NG_012886.2:g.343005del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.12387+326del MANE Select	ENSP00000475939.1:n.12387+326del
ENST00000328843.10:c.12408+326del	ENSP00000330671.7:n.12408+326del
ENST00000409508.7:c.12387+326del	ENSP00000475939.1:n.12387+326del
ENST00000620169.4:c.12408+326del	ENSP00000481693.1:n.12408+326del
NM_001277115.1:c.12387+326del	NP_001264044.1:n.12387+326del
NM_001277115.2:c.12387+326del MANE Select	NP_001264044.1:n.12387+326del