Canonical Allele Identifier: CA1693666297
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816547A= , CM000669.2:g.21816547A= GRCh38
NC_000007.13:g.21856165A= , CM000669.1:g.21856165A= GRCh37
NC_000007.12:g.21822690A= NCBI36
NG_012886.2:g.278333A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10413A= MANE Select ENSP00000475939.1:p.Glu3471=
ENST00000328843.10:c.10434A= ENSP00000330671.7:p.Glu3478=
ENST00000409508.7:c.10413A= ENSP00000475939.1:p.Glu3471=
ENST00000620169.4:c.10434A= ENSP00000481693.1:p.Glu3478=
NM_001277115.1:c.10413A= NP_001264044.1:p.Glu3471=
NM_001277115.2:c.10413A= MANE Select NP_001264044.1:p.Glu3471=
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