Canonical Allele Identifier: CA1693626774
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21705564A= , CM000669.2:g.21705564A= GRCh38
NC_000007.13:g.21745182A= , CM000669.1:g.21745182A= GRCh37
NC_000007.12:g.21711707A= NCBI36
NG_012886.2:g.167350A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.6546+27A= MANE Select ENSP00000475939.1:n.6546+27A=
ENST00000328843.10:c.6567+27A= ENSP00000330671.7:n.6567+27A=
ENST00000409508.7:c.6546+27A= ENSP00000475939.1:n.6546+27A=
ENST00000620169.4:c.6567+27A= ENSP00000481693.1:n.6567+27A=
NM_001277115.1:c.6546+27A= NP_001264044.1:n.6546+27A=
NM_001277115.2:c.6546+27A= MANE Select NP_001264044.1:n.6546+27A=
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