Canonical Allele Identifier: CA1693605609
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1782345300
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21664339C>T , CM000669.2:g.21664339C>T GRCh38
NC_000007.13:g.21703957C>T , CM000669.1:g.21703957C>T GRCh37
NC_000007.12:g.21670482C>T NCBI36
NG_012886.2:g.126125C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.5328+5308C>T MANE Select ENSP00000475939.1:n.5328+5308C>T
ENST00000328843.10:c.5343+5308C>T ENSP00000330671.7:n.5343+5308C>T
ENST00000409508.7:c.5328+5308C>T ENSP00000475939.1:n.5328+5308C>T
ENST00000620169.4:c.5343+5308C>T ENSP00000481693.1:n.5343+5308C>T
NM_001277115.1:c.5328+5308C>T NP_001264044.1:n.5328+5308C>T
NM_001277115.2:c.5328+5308C>T MANE Select NP_001264044.1:n.5328+5308C>T
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