Canonical Allele Identifier: CA1693571581
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21619145G= , CM000669.2:g.21619145G= GRCh38
NC_000007.13:g.21658763G= , CM000669.1:g.21658763G= GRCh37
NC_000007.12:g.21625288G= NCBI36
NG_012886.2:g.80931G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.4300G= MANE Select ENSP00000475939.1:p.Ala1434=
ENST00000328843.10:c.4315G= ENSP00000330671.7:p.Ala1439=
ENST00000409508.7:c.4300G= ENSP00000475939.1:p.Ala1434=
ENST00000465593.1:n.326G=
ENST00000620169.4:c.4315G= ENSP00000481693.1:p.Ala1439=
NM_001277115.1:c.4300G= NP_001264044.1:p.Ala1434=
NM_001277115.2:c.4300G= MANE Select NP_001264044.1:p.Ala1434=
Search 100 bp 5'
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