Canonical Allele Identifier: CA1693539323
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21558892A= , CM000669.2:g.21558892A= GRCh38
NC_000007.13:g.21598510A= , CM000669.1:g.21598510A= GRCh37
NC_000007.12:g.21565035A= NCBI36
NG_012886.2:g.20678A=

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.586A= MANE Select ENSP00000475939.1:p.Lys196=
ENST00000328843.10:c.586A= ENSP00000330671.7:p.Lys196=
ENST00000409508.7:c.586A= ENSP00000475939.1:p.Lys196=
ENST00000620169.4:c.586A= ENSP00000481693.1:p.Lys196=
NM_001277115.1:c.586A= NP_001264044.1:p.Lys196=
NM_001277115.2:c.586A= MANE Select NP_001264044.1:p.Lys196=
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