Canonical Allele Identifier: CA1364817291
Gene: DNAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52353589A= , CM000665.2:g.52353589A= GRCh38
NC_000003.11:g.52387605A= , CM000665.1:g.52387605A= GRCh37
NC_000003.10:g.52362645A= NCBI36
NG_052911.1:g.42271A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000420323.7:c.3436A= MANE Select ENSP00000401514.2:p.Ser1146=
ENST00000420323.6:c.3436A= ENSP00000401514.2:p.Ser1146=
ENST00000486752.5:n.3697A=
ENST00000497875.1:n.3601A=
NM_015512.4:c.3436A= NP_056327.4:p.Ser1146=
XM_011533577.1:c.3436A= XP_011531879.1:p.Ser1146=
XM_017006129.1:c.3436A= XP_016861618.1:p.Ser1146=
XM_017006130.1:c.3436A= XP_016861619.1:p.Ser1146=
XM_017006131.1:c.3436A= XP_016861620.1:p.Ser1146=
XM_017006132.1:c.3436A= XP_016861621.1:p.Ser1146=
XM_017006133.1:c.3436A= XP_016861622.1:p.Ser1146=
XR_001740098.1:n.6585A=
XR_001740099.1:n.6585A=
NM_015512.5:c.3436A= MANE Select NP_056327.4:p.Ser1146=