Canonical Allele Identifier: CA2681992314
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21880930-TTTACAAAGCTGTCAGTCTTTGGGCACTATCAAAATTGA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880931_21880968del , CM000669.2:g.21880931_21880968del GRCh38
NC_000007.13:g.21920549_21920586del , CM000669.1:g.21920549_21920586del GRCh37
NC_000007.12:g.21887074_21887111del NCBI36
NG_012886.2:g.342717_342754del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12387+38_12387+75del MANE Select ENSP00000475939.1:n.12387+38_12387+75del
ENST00000328843.10:c.12408+38_12408+75del ENSP00000330671.7:n.12408+38_12408+75del
ENST00000409508.7:c.12387+38_12387+75del ENSP00000475939.1:n.12387+38_12387+75del
ENST00000620169.4:c.12408+38_12408+75del ENSP00000481693.1:n.12408+38_12408+75del
NM_001277115.1:c.12387+38_12387+75del NP_001264044.1:n.12387+38_12387+75del
NM_001277115.2:c.12387+38_12387+75del MANE Select NP_001264044.1:n.12387+38_12387+75del
Search 100 bp 5'
Search 100 bp 3'