Canonical Allele Identifier: CA155159344

Gene: DNAH11

Linked Data

• dbSNP Id: rs769260416
• MyVariant Identifiers: chr7:g.21920850del (hg19) ; chr7:g.21881232del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21881233del , CM000669.2:g.21881233del	GRCh38
NC_000007.13:g.21920851del , CM000669.1:g.21920851del	GRCh37
NC_000007.12:g.21887376del	NCBI36
NG_012886.2:g.343019del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.12387+340del MANE Select	ENSP00000475939.1:n.12387+340del
ENST00000328843.10:c.12408+340del	ENSP00000330671.7:n.12408+340del
ENST00000409508.7:c.12387+340del	ENSP00000475939.1:n.12387+340del
ENST00000620169.4:c.12408+340del	ENSP00000481693.1:n.12408+340del
NM_001277115.1:c.12387+340del	NP_001264044.1:n.12387+340del
NM_001277115.2:c.12387+340del MANE Select	NP_001264044.1:n.12387+340del