Canonical Allele Identifier: CA398152899

Gene: DNAH9

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.11598501G>A , CM000679.2:g.11598501G>A	GRCh38
NC_000017.10:g.11501818G>A , CM000679.1:g.11501818G>A	GRCh37
NC_000017.9:g.11442543G>A	NCBI36
NG_047047.1:g.5071G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001372.4:c.3G>A MANE Select	NP_001363.2:p.Met1Ile
ENST00000262442.9:c.3G>A MANE Select	ENSP00000262442.3:p.Met1Ile
NM_001372.3:c.3G>A	NP_001363.2:p.Met1Ile
ENST00000262442.8:c.3G>A	ENSP00000262442.3:p.Met1Ile
ENST00000454412.6:c.3G>A	ENSP00000414874.2:p.Met1Ile
ENST00000579406.1:n.30G>A
ENST00000579828.5:c.3G>A	ENSP00000463782.1:p.Met1Ile
XM_011523703.1:c.3G>A	XP_011522005.1:p.Met1Ile
XM_011523703.2:c.3G>A	XP_011522005.1:p.Met1Ile
XM_017024292.2:c.3G>A	XP_016879781.1:p.Met1Ile
XM_017024294.2:c.3G>A	XP_016879783.1:p.Met1Ile
XM_017024295.2:c.3G>A	XP_016879784.1:p.Met1Ile