Canonical Allele Identifier: CA8395074
Community Standard Title: NM_001372.4(DNAH9):c.2066C>T (p.Thr689Met)
Gene: DNAH9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.11647167C>T , CM000679.2:g.11647167C>T GRCh38
NC_000017.10:g.11550484C>T , CM000679.1:g.11550484C>T GRCh37
NC_000017.9:g.11491209C>T NCBI36
NG_047047.1:g.53737C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001372.4:c.2066C>T MANE Select NP_001363.2:p.Thr689Met
ENST00000262442.9:c.2066C>T MANE Select ENSP00000262442.3:p.Thr689Met
NM_001372.3:c.2066C>T NP_001363.2:p.Thr689Met
ENST00000262442.8:c.2066C>T ENSP00000262442.3:p.Thr689Met
ENST00000454412.6:c.2066C>T ENSP00000414874.2:p.Thr689Met
XM_011523703.1:c.2066C>T XP_011522005.1:p.Thr689Met
XM_011523703.2:c.2066C>T XP_011522005.1:p.Thr689Met
XM_017024292.2:c.1949C>T XP_016879781.1:p.Thr650Met
XM_017024293.1:c.-21-3902C>T XP_016879782.1:n.-21-3902C>T
XM_017024294.2:c.2066C>T XP_016879783.1:p.Thr689Met
XM_017024295.2:c.2066C>T XP_016879784.1:p.Thr689Met