Canonical Allele Identifier: CA1693713189
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21881235C= , CM000669.2:g.21881235C= GRCh38
NC_000007.13:g.21920853C= , CM000669.1:g.21920853C= GRCh37
NC_000007.12:g.21887378C= NCBI36
NG_012886.2:g.343021C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12387+342C= MANE Select ENSP00000475939.1:n.12387+342C=
ENST00000328843.10:c.12408+342C= ENSP00000330671.7:n.12408+342C=
ENST00000409508.7:c.12387+342C= ENSP00000475939.1:n.12387+342C=
ENST00000620169.4:c.12408+342C= ENSP00000481693.1:n.12408+342C=
NM_001277115.1:c.12387+342C= NP_001264044.1:n.12387+342C=
NM_001277115.2:c.12387+342C= MANE Select NP_001264044.1:n.12387+342C=
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