Canonical Allele Identifier: CA1693539918
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21559123A= , CM000669.2:g.21559123A= GRCh38
NC_000007.13:g.21598741A= , CM000669.1:g.21598741A= GRCh37
NC_000007.12:g.21565266A= NCBI36
NG_012886.2:g.20909A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.692+125A= MANE Select ENSP00000475939.1:n.692+125A=
ENST00000328843.10:c.692+125A= ENSP00000330671.7:n.692+125A=
ENST00000409508.7:c.692+125A= ENSP00000475939.1:n.692+125A=
ENST00000620169.4:c.692+125A= ENSP00000481693.1:n.692+125A=
NM_001277115.1:c.692+125A= NP_001264044.1:n.692+125A=
NM_001277115.2:c.692+125A= MANE Select NP_001264044.1:n.692+125A=
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