Canonical Allele Identifier: CA1693666470
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816624A= , CM000669.2:g.21816624A= GRCh38
NC_000007.13:g.21856242A= , CM000669.1:g.21856242A= GRCh37
NC_000007.12:g.21822767A= NCBI36
NG_012886.2:g.278410A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10490A= MANE Select ENSP00000475939.1:p.Asp3497=
ENST00000328843.10:c.10511A= ENSP00000330671.7:p.Asp3504=
ENST00000409508.7:c.10490A= ENSP00000475939.1:p.Asp3497=
ENST00000620169.4:c.10511A= ENSP00000481693.1:p.Asp3504=
NM_001277115.1:c.10490A= NP_001264044.1:p.Asp3497=
NM_001277115.2:c.10490A= MANE Select NP_001264044.1:p.Asp3497=