Canonical Allele Identifier: CA2433823
Community Standard Title: NM_015512.5(DNAH1):c.4167C>A (p.Tyr1389Ter)
Gene: DNAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52358638C>A , CM000665.2:g.52358638C>A GRCh38
NC_000003.11:g.52392654C>A , CM000665.1:g.52392654C>A GRCh37
NC_000003.10:g.52367694C>A NCBI36
NG_052911.1:g.47320C>A

Transcript Alleles

HGVS Amino-acid Change
NM_015512.5:c.4167C>A MANE Select NP_056327.4:p.Tyr1389Ter
ENST00000420323.7:c.4167C>A MANE Select ENSP00000401514.2:p.Tyr1389Ter
NM_015512.4:c.4167C>A NP_056327.4:p.Tyr1389Ter
ENST00000420323.6:c.4167C>A ENSP00000401514.2:p.Tyr1389Ter
ENST00000486752.5:n.4428C>A
XM_011533577.1:c.4167C>A XP_011531879.1:p.Tyr1389Ter
XM_017006129.1:c.4167C>A XP_016861618.1:p.Tyr1389Ter
XM_017006130.1:c.4167C>A XP_016861619.1:p.Tyr1389Ter
XM_017006131.1:c.4167C>A XP_016861620.1:p.Tyr1389Ter
XM_017006132.1:c.4167C>A XP_016861621.1:p.Tyr1389Ter
XM_017006133.1:c.4167C>A XP_016861622.1:p.Tyr1389Ter
XR_001740098.1:n.7316C>A
XR_001740099.1:n.7316C>A