Canonical Allele Identifier: CA1693662150
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748734G= , CM000669.2:g.21748734G= GRCh38
NC_000007.13:g.21788352G= , CM000669.1:g.21788352G= GRCh37
NC_000007.12:g.21754877G= NCBI36
NG_012886.2:g.210520G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8665G= MANE Select ENSP00000475939.1:p.Glu2889=
ENST00000328843.10:c.8686G= ENSP00000330671.7:p.Glu2896=
ENST00000409508.7:c.8665G= ENSP00000475939.1:p.Glu2889=
ENST00000620169.4:c.8686G= ENSP00000481693.1:p.Glu2896=
NM_001277115.1:c.8665G= NP_001264044.1:p.Glu2889=
NM_001277115.2:c.8665G= MANE Select NP_001264044.1:p.Glu2889=
Search 100 bp 5'
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