Canonical Allele Identifier: CA398212824
Community Standard Title: NM_001372.4(DNAH9):c.12106-1G>A
Gene: DNAH9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.11932013G>A , CM000679.2:g.11932013G>A GRCh38
NC_000017.10:g.11835330G>A , CM000679.1:g.11835330G>A GRCh37
NC_000017.9:g.11776055G>A NCBI36
NG_047047.1:g.338583G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001372.4:c.12106-1G>A MANE Select NP_001363.2:n.12106-1G>A
ENST00000262442.9:c.12106-1G>A MANE Select ENSP00000262442.3:n.12106-1G>A
NM_001372.3:c.12106-1G>A NP_001363.2:n.12106-1G>A
NM_004662.2:c.1042-1G>A NP_004653.2:n.1042-1G>A
ENST00000262442.8:c.12106-1G>A ENSP00000262442.3:n.12106-1G>A
ENST00000396001.6:n.1569-1G>A
ENST00000454412.6:c.11878-1G>A ENSP00000414874.2:n.11878-1G>A
ENST00000608377.5:c.1042-1G>A ENSP00000476951.1:n.1042-1G>A
XM_011523703.1:c.12106-1G>A XP_011522005.1:n.12106-1G>A
XM_011523703.2:c.12106-1G>A XP_011522005.1:n.12106-1G>A
XM_017024292.2:c.11989-1G>A XP_016879781.1:n.11989-1G>A
XM_017024293.1:c.9988-1G>A XP_016879782.1:n.9988-1G>A