Canonical Allele Identifier: CA1693712630
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880743C= , CM000669.2:g.21880743C= GRCh38
NC_000007.13:g.21920361C= , CM000669.1:g.21920361C= GRCh37
NC_000007.12:g.21886886C= NCBI36
NG_012886.2:g.342529C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12237C= MANE Select ENSP00000475939.1:p.Ser4079=
ENST00000328843.10:c.12258C= ENSP00000330671.7:p.Ser4086=
ENST00000409508.7:c.12237C= ENSP00000475939.1:p.Ser4079=
ENST00000620169.4:c.12258C= ENSP00000481693.1:p.Ser4086=
NM_001277115.1:c.12237C= NP_001264044.1:p.Ser4079=
NM_001277115.2:c.12237C= MANE Select NP_001264044.1:p.Ser4079=