Canonical Allele Identifier: CA287796723
Community Standard Title: NM_001372.4(DNAH9):c.235A>G (p.Arg79Gly)
Gene: DNAH9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.11598733A>G , CM000679.2:g.11598733A>G GRCh38
NC_000017.10:g.11502050A>G , CM000679.1:g.11502050A>G GRCh37
NC_000017.9:g.11442775A>G NCBI36
NG_047047.1:g.5303A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001372.4:c.235A>G MANE Select NP_001363.2:p.Arg79Gly
ENST00000262442.9:c.235A>G MANE Select ENSP00000262442.3:p.Arg79Gly
NM_001372.3:c.235A>G NP_001363.2:p.Arg79Gly
ENST00000262442.8:c.235A>G ENSP00000262442.3:p.Arg79Gly
ENST00000454412.6:c.235A>G ENSP00000414874.2:p.Arg79Gly
ENST00000579406.1:n.262A>G
ENST00000579828.5:c.235A>G ENSP00000463782.1:p.Arg79Gly
XM_011523703.1:c.235A>G XP_011522005.1:p.Arg79Gly
XM_011523703.2:c.235A>G XP_011522005.1:p.Arg79Gly
XM_017024292.2:c.235A>G XP_016879781.1:p.Arg79Gly
XM_017024294.2:c.235A>G XP_016879783.1:p.Arg79Gly
XM_017024295.2:c.235A>G XP_016879784.1:p.Arg79Gly