Canonical Allele Identifier: CA1693666383
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816589C= , CM000669.2:g.21816589C= GRCh38
NC_000007.13:g.21856207C= , CM000669.1:g.21856207C= GRCh37
NC_000007.12:g.21822732C= NCBI36
NG_012886.2:g.278375C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10455C= MANE Select ENSP00000475939.1:p.Ile3485=
ENST00000328843.10:c.10476C= ENSP00000330671.7:p.Ile3492=
ENST00000409508.7:c.10455C= ENSP00000475939.1:p.Ile3485=
ENST00000620169.4:c.10476C= ENSP00000481693.1:p.Ile3492=
NM_001277115.1:c.10455C= NP_001264044.1:p.Ile3485=
NM_001277115.2:c.10455C= MANE Select NP_001264044.1:p.Ile3485=
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