Canonical Allele Identifier: CA1693626640
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21705518C= , CM000669.2:g.21705518C= GRCh38
NC_000007.13:g.21745136C= , CM000669.1:g.21745136C= GRCh37
NC_000007.12:g.21711661C= NCBI36
NG_012886.2:g.167304C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.6527C= MANE Select ENSP00000475939.1:p.Ala2176=
ENST00000328843.10:c.6548C= ENSP00000330671.7:p.Ala2183=
ENST00000409508.7:c.6527C= ENSP00000475939.1:p.Ala2176=
ENST00000620169.4:c.6548C= ENSP00000481693.1:p.Ala2183=
NM_001277115.1:c.6527C= NP_001264044.1:p.Ala2176=
NM_001277115.2:c.6527C= MANE Select NP_001264044.1:p.Ala2176=