Canonical Allele Identifier: CA1693712952
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880971A= , CM000669.2:g.21880971A= GRCh38
NC_000007.13:g.21920589A= , CM000669.1:g.21920589A= GRCh37
NC_000007.12:g.21887114A= NCBI36
NG_012886.2:g.342757A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12387+78A= MANE Select ENSP00000475939.1:n.12387+78A=
ENST00000328843.10:c.12408+78A= ENSP00000330671.7:n.12408+78A=
ENST00000409508.7:c.12387+78A= ENSP00000475939.1:n.12387+78A=
ENST00000620169.4:c.12408+78A= ENSP00000481693.1:n.12408+78A=
NM_001277115.1:c.12387+78A= NP_001264044.1:n.12387+78A=
NM_001277115.2:c.12387+78A= MANE Select NP_001264044.1:n.12387+78A=
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