Canonical Allele Identifier: CA2714084373
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs2128467405
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21664308A>G , CM000669.2:g.21664308A>G GRCh38
NC_000007.13:g.21703926A>G , CM000669.1:g.21703926A>G GRCh37
NC_000007.12:g.21670451A>G NCBI36
NG_012886.2:g.126094A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.5328+5277A>G MANE Select ENSP00000475939.1:n.5328+5277A>G
ENST00000328843.10:c.5343+5277A>G ENSP00000330671.7:n.5343+5277A>G
ENST00000409508.7:c.5328+5277A>G ENSP00000475939.1:n.5328+5277A>G
ENST00000620169.4:c.5343+5277A>G ENSP00000481693.1:n.5343+5277A>G
NM_001277115.1:c.5328+5277A>G NP_001264044.1:n.5328+5277A>G
NM_001277115.2:c.5328+5277A>G MANE Select NP_001264044.1:n.5328+5277A>G
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