Canonical Allele Identifier: CA2673269751
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13769220_13769228del , CM000667.2:g.13769220_13769228del GRCh38
NC_000005.9:g.13769329_13769337del , CM000667.1:g.13769329_13769337del GRCh37
NC_000005.8:g.13822329_13822337del NCBI36
NG_013081.1:g.180259_180267del
NG_013081.2:g.180259_180267del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9721-86_9721-78del MANE Select ENSP00000265104.4:n.9721-86_9721-78del
ENST00000681290.1:c.9676-86_9676-78del ENSP00000505288.1:n.9676-86_9676-78del
ENST00000265104.4:c.9721-86_9721-78del ENSP00000265104.4:n.9721-86_9721-78del
ENST00000504001.3:n.433-86_433-78del
NM_001369.2:c.9721-86_9721-78del NP_001360.1:n.9721-86_9721-78del
XM_005248262.2:c.9676-86_9676-78del XP_005248319.1:n.9676-86_9676-78del
XM_005248262.3:c.9829-86_9829-78del XP_005248319.2:n.9829-86_9829-78del
XM_017009177.1:c.9829-86_9829-78del XP_016864666.1:n.9829-86_9829-78del
XM_017009178.1:c.8734-86_8734-78del XP_016864667.1:n.8734-86_8734-78del
XM_017009179.2:c.8734-86_8734-78del XP_016864668.1:n.8734-86_8734-78del
XM_017009180.1:c.9829-86_9829-78del XP_016864669.1:n.9829-86_9829-78del
XM_017009181.1:c.9829-86_9829-78del XP_016864670.1:n.9829-86_9829-78del
XM_017009182.1:c.9829-86_9829-78del XP_016864671.1:n.9829-86_9829-78del
XM_017009185.1:c.4918-86_4918-78del XP_016864674.1:n.4918-86_4918-78del
XM_017009186.1:c.4471-86_4471-78del XP_016864675.1:n.4471-86_4471-78del
XM_017009188.1:c.3808-86_3808-78del XP_016864677.1:n.3808-86_3808-78del
XM_024454388.1:c.8734-86_8734-78del XP_024310156.1:n.8734-86_8734-78del
XM_024454389.1:c.8323-86_8323-78del XP_024310157.1:n.8323-86_8323-78del
NM_001369.3:c.9721-86_9721-78del MANE Select NP_001360.1:n.9721-86_9721-78del