Canonical Allele Identifier: CA2433433
Community Standard Title: NM_015512.5(DNAH1):c.2926G>A (p.Ala976Thr)
Gene: DNAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52352606G>A , CM000665.2:g.52352606G>A GRCh38
NC_000003.11:g.52386622G>A , CM000665.1:g.52386622G>A GRCh37
NC_000003.10:g.52361662G>A NCBI36
NG_052911.1:g.41288G>A

Transcript Alleles

HGVS Amino-acid Change
NM_015512.5:c.2926G>A MANE Select NP_056327.4:p.Ala976Thr
ENST00000420323.7:c.2926G>A MANE Select ENSP00000401514.2:p.Ala976Thr
NM_015512.4:c.2926G>A NP_056327.4:p.Ala976Thr
ENST00000420323.6:c.2926G>A ENSP00000401514.2:p.Ala976Thr
ENST00000486752.5:n.3187G>A
ENST00000497875.1:n.3091G>A
XM_011533577.1:c.2926G>A XP_011531879.1:p.Ala976Thr
XM_017006129.1:c.2926G>A XP_016861618.1:p.Ala976Thr
XM_017006130.1:c.2926G>A XP_016861619.1:p.Ala976Thr
XM_017006131.1:c.2926G>A XP_016861620.1:p.Ala976Thr
XM_017006132.1:c.2926G>A XP_016861621.1:p.Ala976Thr
XM_017006133.1:c.2926G>A XP_016861622.1:p.Ala976Thr
XR_001740098.1:n.6075G>A
XR_001740099.1:n.6075G>A