Canonical Allele Identifier: CA1693571628
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21619155_21619157delinsTAC , CM000669.2:g.21619155_21619157delinsTAC GRCh38
NC_000007.13:g.21658773_21658775delinsTAC , CM000669.1:g.21658773_21658775delinsTAC GRCh37
NC_000007.12:g.21625298_21625300delinsTAC NCBI36
NG_012886.2:g.80941_80943delinsTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.4310_4312delinsTAC MANE Select ENSP00000475939.1:p.Leu1437=
ENST00000328843.10:c.4325_4327delinsTAC ENSP00000330671.7:p.Leu1442=
ENST00000409508.7:c.4310_4312delinsTAC ENSP00000475939.1:p.Leu1437=
ENST00000465593.1:n.336_338delinsTAC
ENST00000620169.4:c.4325_4327delinsTAC ENSP00000481693.1:p.Leu1442=
NM_001277115.1:c.4310_4312delinsTAC NP_001264044.1:p.Leu1437=
NM_001277115.2:c.4310_4312delinsTAC MANE Select NP_001264044.1:p.Leu1437=
Search 100 bp 5'
Search 100 bp 3'