Canonical Allele Identifier: CA8396429
Community Standard Title: NM_001372.4(DNAH9):c.6847+1G>A
Gene: DNAH9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.11756677G>A , CM000679.2:g.11756677G>A GRCh38
NC_000017.10:g.11659994G>A , CM000679.1:g.11659994G>A GRCh37
NC_000017.9:g.11600719G>A NCBI36
NG_047047.1:g.163247G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001372.4:c.6847+1G>A MANE Select NP_001363.2:n.6847+1G>A
ENST00000262442.9:c.6847+1G>A MANE Select ENSP00000262442.3:n.6847+1G>A
NM_001372.3:c.6847+1G>A NP_001363.2:n.6847+1G>A
ENST00000262442.8:c.6847+1G>A ENSP00000262442.3:n.6847+1G>A
ENST00000454412.6:c.6847+1G>A ENSP00000414874.2:n.6847+1G>A
XM_011523703.1:c.6847+1G>A XP_011522005.1:n.6847+1G>A
XM_011523703.2:c.6847+1G>A XP_011522005.1:n.6847+1G>A
XM_017024292.2:c.6730+1G>A XP_016879781.1:n.6730+1G>A
XM_017024293.1:c.4729+1G>A XP_016879782.1:n.4729+1G>A
XM_017024294.2:c.6847+1G>A XP_016879783.1:n.6847+1G>A
XM_017024295.2:c.6847+1G>A XP_016879784.1:n.6847+1G>A