Canonical Allele Identifier: CA1693666267
Gene: DNAH11 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816532C= , CM000669.2:g.21816532C= GRCh38
NC_000007.13:g.21856150C= , CM000669.1:g.21856150C= GRCh37
NC_000007.12:g.21822675C= NCBI36
NG_012886.2:g.278318C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10398C= MANE Select ENSP00000475939.1:p.Ala3466=
ENST00000328843.10:c.10419C= ENSP00000330671.7:p.Ala3473=
ENST00000409508.7:c.10398C= ENSP00000475939.1:p.Ala3466=
ENST00000620169.4:c.10419C= ENSP00000481693.1:p.Ala3473=
NM_001277115.1:c.10398C= NP_001264044.1:p.Ala3466=
NM_001277115.2:c.10398C= MANE Select NP_001264044.1:p.Ala3466=
Search 100 bp 5'
Search 100 bp 3'