Canonical Allele Identifier: CA1693539669
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21558998_21559002delinsAGTAC , CM000669.2:g.21558998_21559002delinsAGTAC GRCh38
NC_000007.13:g.21598616_21598620delinsAGTAC , CM000669.1:g.21598616_21598620delinsAGTAC GRCh37
NC_000007.12:g.21565141_21565145delinsAGTAC NCBI36
NG_012886.2:g.20784_20788delinsAGTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.692_692+4delinsAGTAC
ENST00000328843.10:c.692_692+4delinsAGTAC
ENST00000409508.7:c.692_692+4delinsAGTAC
ENST00000620169.4:c.692_692+4delinsAGTAC
NM_001277115.1:c.692_692+4delinsAGTAC
NM_001277115.2:c.692_692+4delinsAGTAC