Canonical Allele Identifier: CA8397257
Gene: DNAH9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.11854038G>A , CM000679.2:g.11854038G>A GRCh38
NC_000017.10:g.11757355G>A , CM000679.1:g.11757355G>A GRCh37
NC_000017.9:g.11698080G>A NCBI36
NG_047047.1:g.260608G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001372.4:c.9543G>A MANE Select NP_001363.2:p.Pro3181=
ENST00000262442.9:c.9543G>A MANE Select ENSP00000262442.3:p.Pro3181=
NM_001372.3:c.9543G>A NP_001363.2:p.Pro3181=
ENST00000262442.8:c.9543G>A ENSP00000262442.3:p.Pro3181=
ENST00000454412.6:c.9543G>A ENSP00000414874.2:p.Pro3181=
ENST00000578834.1:n.90G>A
XM_011523703.1:c.9543G>A XP_011522005.1:p.Pro3181=
XM_011523703.2:c.9543G>A XP_011522005.1:p.Pro3181=
XM_017024292.2:c.9426G>A XP_016879781.1:p.Pro3142=
XM_017024293.1:c.7425G>A XP_016879782.1:p.Pro2475=
XM_017024294.2:c.9543G>A XP_016879783.1:p.Pro3181=