Canonical Allele Identifier: CA2695207509
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748580_21748583delinsATCCG , CM000669.2:g.21748580_21748583delinsATCCG GRCh38
NC_000007.13:g.21788198_21788201delinsATCCG , CM000669.1:g.21788198_21788201delinsATCCG GRCh37
NC_000007.12:g.21754723_21754726delinsATCCG NCBI36
NG_012886.2:g.210366_210369delinsATCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8511_8514delinsATCCG MANE Select ENSP00000475939.1:p.Cys2838SerfsTer?
ENST00000328843.10:c.8532_8535delinsATCCG ENSP00000330671.7:p.Cys2845SerfsTer?
ENST00000409508.7:c.8511_8514delinsATCCG ENSP00000475939.1:p.Cys2838SerfsTer?
ENST00000620169.4:c.8532_8535delinsATCCG ENSP00000481693.1:p.Cys2845SerfsTer?
NM_001277115.1:c.8511_8514delinsATCCG NP_001264044.1:p.Cys2838SerfsTer?
NM_001277115.2:c.8511_8514delinsATCCG MANE Select NP_001264044.1:p.Cys2838SerfsTer?