Canonical Allele Identifier: CA398160412
Community Standard Title: NM_001372.4(DNAH9):c.615-2A>G
Gene: DNAH9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.11610394A>G , CM000679.2:g.11610394A>G GRCh38
NC_000017.10:g.11513711A>G , CM000679.1:g.11513711A>G GRCh37
NC_000017.9:g.11454436A>G NCBI36
NG_047047.1:g.16964A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001372.4:c.615-2A>G MANE Select NP_001363.2:n.615-2A>G
ENST00000262442.9:c.615-2A>G MANE Select ENSP00000262442.3:n.615-2A>G
NM_001372.3:c.615-2A>G NP_001363.2:n.615-2A>G
ENST00000262442.8:c.615-2A>G ENSP00000262442.3:n.615-2A>G
ENST00000454412.6:c.615-2A>G ENSP00000414874.2:n.615-2A>G
ENST00000579406.1:n.642-2A>G
ENST00000579828.5:c.615-2A>G ENSP00000463782.1:n.615-2A>G
XM_011523703.1:c.615-2A>G XP_011522005.1:n.615-2A>G
XM_011523703.2:c.615-2A>G XP_011522005.1:n.615-2A>G
XM_017024292.2:c.615-2A>G XP_016879781.1:n.615-2A>G
XM_017024294.2:c.615-2A>G XP_016879783.1:n.615-2A>G
XM_017024295.2:c.615-2A>G XP_016879784.1:n.615-2A>G