Canonical Allele Identifier: CA1693537974
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21543351G= , CM000669.2:g.21543351G= GRCh38
NC_000007.13:g.21582969G= , CM000669.1:g.21582969G= GRCh37
NC_000007.12:g.21549494G= NCBI36
NG_012886.2:g.5137G=

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.106G= MANE Select ENSP00000475939.1:p.Glu36=
ENST00000328843.10:c.106G= ENSP00000330671.7:p.Glu36=
ENST00000409508.7:c.106G= ENSP00000475939.1:p.Glu36=
ENST00000620169.4:c.106G= ENSP00000481693.1:p.Glu36=
NM_001277115.1:c.106G= NP_001264044.1:p.Glu36=
NM_001277115.2:c.106G= MANE Select NP_001264044.1:p.Glu36=