Canonical Allele Identifier: CA1693713196
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21881244A= , CM000669.2:g.21881244A= GRCh38
NC_000007.13:g.21920862A= , CM000669.1:g.21920862A= GRCh37
NC_000007.12:g.21887387A= NCBI36
NG_012886.2:g.343030A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12387+351A= MANE Select ENSP00000475939.1:n.12387+351A=
ENST00000328843.10:c.12408+351A= ENSP00000330671.7:n.12408+351A=
ENST00000409508.7:c.12387+351A= ENSP00000475939.1:n.12387+351A=
ENST00000620169.4:c.12408+351A= ENSP00000481693.1:n.12408+351A=
NM_001277115.1:c.12387+351A= NP_001264044.1:n.12387+351A=
NM_001277115.2:c.12387+351A= MANE Select NP_001264044.1:n.12387+351A=
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