Canonical Allele Identifier: CA1693571552
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21619134_21619135delinsCA , CM000669.2:g.21619134_21619135delinsCA GRCh38
NC_000007.13:g.21658752_21658753delinsCA , CM000669.1:g.21658752_21658753delinsCA GRCh37
NC_000007.12:g.21625277_21625278delinsCA NCBI36
NG_012886.2:g.80920_80921delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.4289_4290delinsCA MANE Select ENSP00000475939.1:p.Ala1430=
ENST00000328843.10:c.4304_4305delinsCA ENSP00000330671.7:p.Ala1435=
ENST00000409508.7:c.4289_4290delinsCA ENSP00000475939.1:p.Ala1430=
ENST00000465593.1:n.315_316delinsCA
ENST00000620169.4:c.4304_4305delinsCA ENSP00000481693.1:p.Ala1435=
NM_001277115.1:c.4289_4290delinsCA NP_001264044.1:p.Ala1430=
NM_001277115.2:c.4289_4290delinsCA MANE Select NP_001264044.1:p.Ala1430=
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