Canonical Allele Identifier: CA1693578831

Gene: DNAH11

Linked Data

• dbSNP Id: rs1784998067
• gnomAD v4: 7-21599721-GGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21599725_21599726del , CM000669.2:g.21599725_21599726del	GRCh38
NC_000007.13:g.21639343_21639344del , CM000669.1:g.21639343_21639344del	GRCh37
NC_000007.12:g.21605868_21605869del	NCBI36
NG_012886.2:g.61511_61512del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.2668-62_2668-61del MANE Select	ENSP00000475939.1:n.2668-62_2668-61del
ENST00000328843.10:c.2668-62_2668-61del	ENSP00000330671.7:n.2668-62_2668-61del
ENST00000409508.7:c.2668-62_2668-61del	ENSP00000475939.1:n.2668-62_2668-61del
ENST00000620169.4:c.2668-62_2668-61del	ENSP00000481693.1:n.2668-62_2668-61del
NM_001277115.1:c.2668-62_2668-61del	NP_001264044.1:n.2668-62_2668-61del
NM_001277115.2:c.2668-62_2668-61del MANE Select	NP_001264044.1:n.2668-62_2668-61del