Canonical Allele Identifier: CA2432878
Community Standard Title: NM_015512.5(DNAH1):c.1114G>A (p.Ala372Thr)
Gene: DNAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52332222G>A , CM000665.2:g.52332222G>A GRCh38
NC_000003.11:g.52366238G>A , CM000665.1:g.52366238G>A GRCh37
NC_000003.10:g.52341278G>A NCBI36
NG_052911.1:g.20904G>A

Transcript Alleles

HGVS Amino-acid Change
NM_015512.5:c.1114G>A MANE Select NP_056327.4:p.Ala372Thr
ENST00000420323.7:c.1114G>A MANE Select ENSP00000401514.2:p.Ala372Thr
NM_015512.4:c.1114G>A NP_056327.4:p.Ala372Thr
ENST00000420323.6:c.1114G>A ENSP00000401514.2:p.Ala372Thr
ENST00000486752.5:n.1375G>A
ENST00000497875.1:n.1279G>A
XM_011533577.1:c.1114G>A XP_011531879.1:p.Ala372Thr
XM_017006129.1:c.1114G>A XP_016861618.1:p.Ala372Thr
XM_017006130.1:c.1114G>A XP_016861619.1:p.Ala372Thr
XM_017006131.1:c.1114G>A XP_016861620.1:p.Ala372Thr
XM_017006132.1:c.1114G>A XP_016861621.1:p.Ala372Thr
XM_017006133.1:c.1114G>A XP_016861622.1:p.Ala372Thr
XR_001740098.1:n.4263G>A
XR_001740099.1:n.4263G>A