Canonical Allele Identifier: CA2247884386
Gene: DNAH9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.11900144C>A , CM000679.2:g.11900144C>A GRCh38
NC_000017.10:g.11803461C>A , CM000679.1:g.11803461C>A GRCh37
NC_000017.9:g.11744186C>A NCBI36
NG_047047.1:g.306714C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262442.9:c.11407-2575C>A MANE Select ENSP00000262442.3:n.11407-2575C>A
ENST00000262442.8:c.11407-2575C>A ENSP00000262442.3:n.11407-2575C>A
ENST00000396001.6:n.870-2575C>A
ENST00000454412.6:c.11407-2575C>A ENSP00000414874.2:n.11407-2575C>A
ENST00000581682.1:n.688-2575C>A
ENST00000608377.5:c.343-2575C>A ENSP00000476951.1:n.343-2575C>A
NM_001372.3:c.11407-2575C>A NP_001363.2:n.11407-2575C>A
NM_004662.2:c.343-2575C>A NP_004653.2:n.343-2575C>A
XM_011523703.1:c.11407-2575C>A XP_011522005.1:n.11407-2575C>A
XM_011523703.2:c.11407-2575C>A XP_011522005.1:n.11407-2575C>A
XM_017024292.2:c.11290-2575C>A XP_016879781.1:n.11290-2575C>A
XM_017024293.1:c.9289-2575C>A XP_016879782.1:n.9289-2575C>A
NM_001372.4:c.11407-2575C>A MANE Select NP_001363.2:n.11407-2575C>A
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