Canonical Allele Identifier: CA1630834688
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21543346A= , CM000669.2:g.21543346A= GRCh38
NC_000007.13:g.21582964A= , CM000669.1:g.21582964A= GRCh37
NC_000007.12:g.21549489A= NCBI36
NG_012886.2:g.5132A=

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.101A= MANE Select ENSP00000475939.1:p.Glu34=
ENST00000328843.10:c.101A= ENSP00000330671.7:p.Glu34=
ENST00000409508.7:c.101A= ENSP00000475939.1:p.Glu34=
ENST00000620169.4:c.101A= ENSP00000481693.1:p.Glu34=
NM_001277115.1:c.101A= NP_001264044.1:p.Glu34=
NM_001277115.2:c.101A= MANE Select NP_001264044.1:p.Glu34=