Canonical Allele Identifier: CA74740020
Community Standard Title: NM_015512.5(DNAH1):c.2254C>T (p.Arg752Ter)
Gene: DNAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52349035C>T , CM000665.2:g.52349035C>T GRCh38
NC_000003.11:g.52383051C>T , CM000665.1:g.52383051C>T GRCh37
NC_000003.10:g.52358091C>T NCBI36
NG_052911.1:g.37717C>T

Transcript Alleles

HGVS Amino-acid Change
NM_015512.5:c.2254C>T MANE Select NP_056327.4:p.Arg752Ter
ENST00000420323.7:c.2254C>T MANE Select ENSP00000401514.2:p.Arg752Ter
NM_015512.4:c.2254C>T NP_056327.4:p.Arg752Ter
ENST00000420323.6:c.2254C>T ENSP00000401514.2:p.Arg752Ter
ENST00000486752.5:n.2515C>T
ENST00000497875.1:n.2419C>T
XM_011533577.1:c.2254C>T XP_011531879.1:p.Arg752Ter
XM_017006129.1:c.2254C>T XP_016861618.1:p.Arg752Ter
XM_017006130.1:c.2254C>T XP_016861619.1:p.Arg752Ter
XM_017006131.1:c.2254C>T XP_016861620.1:p.Arg752Ter
XM_017006132.1:c.2254C>T XP_016861621.1:p.Arg752Ter
XM_017006133.1:c.2254C>T XP_016861622.1:p.Arg752Ter
XR_001740098.1:n.5403C>T
XR_001740099.1:n.5403C>T