Canonical Allele Identifier: CA1693605581
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21664293A= , CM000669.2:g.21664293A= GRCh38
NC_000007.13:g.21703911A= , CM000669.1:g.21703911A= GRCh37
NC_000007.12:g.21670436A= NCBI36
NG_012886.2:g.126079A=

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.5328+5262A= MANE Select ENSP00000475939.1:n.5328+5262A=
ENST00000328843.10:c.5343+5262A= ENSP00000330671.7:n.5343+5262A=
ENST00000409508.7:c.5328+5262A= ENSP00000475939.1:n.5328+5262A=
ENST00000620169.4:c.5343+5262A= ENSP00000481693.1:n.5343+5262A=
NM_001277115.1:c.5328+5262A= NP_001264044.1:n.5328+5262A=
NM_001277115.2:c.5328+5262A= MANE Select NP_001264044.1:n.5328+5262A=
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