Canonical Allele Identifier: CA398190882

Gene: DNAH9

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.11781008G>T , CM000679.2:g.11781008G>T	GRCh38
NC_000017.10:g.11684325G>T , CM000679.1:g.11684325G>T	GRCh37
NC_000017.9:g.11625050G>T	NCBI36
NG_047047.1:g.187578G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001372.4:c.7553-1G>T MANE Select	NP_001363.2:n.7553-1G>T
ENST00000262442.9:c.7553-1G>T MANE Select	ENSP00000262442.3:n.7553-1G>T
NM_001372.3:c.7553-1G>T	NP_001363.2:n.7553-1G>T
ENST00000262442.8:c.7553-1G>T	ENSP00000262442.3:n.7553-1G>T
ENST00000454412.6:c.7553-1G>T	ENSP00000414874.2:n.7553-1G>T
XM_011523703.1:c.7553-1G>T	XP_011522005.1:n.7553-1G>T
XM_011523703.2:c.7553-1G>T	XP_011522005.1:n.7553-1G>T
XM_017024292.2:c.7436-1G>T	XP_016879781.1:n.7436-1G>T
XM_017024293.1:c.5435-1G>T	XP_016879782.1:n.5435-1G>T
XM_017024294.2:c.7553-1G>T	XP_016879783.1:n.7553-1G>T