Canonical Allele Identifier: CA2552290073
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13771190_13771191del , CM000667.2:g.13771190_13771191del GRCh38
NC_000005.9:g.13771299_13771300del , CM000667.1:g.13771299_13771300del GRCh37
NC_000005.8:g.13824299_13824300del NCBI36
NG_013081.1:g.178290_178291del
NG_013081.2:g.178290_178291del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9374-211_9374-210del MANE Select ENSP00000265104.4:n.9374-211_9374-210del
ENST00000681290.1:c.9329-211_9329-210del ENSP00000505288.1:n.9329-211_9329-210del
ENST00000265104.4:c.9374-211_9374-210del ENSP00000265104.4:n.9374-211_9374-210del
ENST00000504001.3:n.85+7_85+8del
NM_001369.2:c.9374-211_9374-210del NP_001360.1:n.9374-211_9374-210del
XM_005248262.2:c.9329-211_9329-210del XP_005248319.1:n.9329-211_9329-210del
XM_005248262.3:c.9482-211_9482-210del XP_005248319.2:n.9482-211_9482-210del
XM_017009177.1:c.9482-211_9482-210del XP_016864666.1:n.9482-211_9482-210del
XM_017009178.1:c.8387-211_8387-210del XP_016864667.1:n.8387-211_8387-210del
XM_017009179.2:c.8387-211_8387-210del XP_016864668.1:n.8387-211_8387-210del
XM_017009180.1:c.9482-211_9482-210del XP_016864669.1:n.9482-211_9482-210del
XM_017009181.1:c.9482-211_9482-210del XP_016864670.1:n.9482-211_9482-210del
XM_017009182.1:c.9482-211_9482-210del XP_016864671.1:n.9482-211_9482-210del
XM_017009183.1:c.9482-211_9482-210del XP_016864672.1:n.9482-211_9482-210del
XM_017009185.1:c.4571-211_4571-210del XP_016864674.1:n.4571-211_4571-210del
XM_017009186.1:c.4124-211_4124-210del XP_016864675.1:n.4124-211_4124-210del
XM_017009188.1:c.3461-211_3461-210del XP_016864677.1:n.3461-211_3461-210del
XM_024454388.1:c.8387-211_8387-210del XP_024310156.1:n.8387-211_8387-210del
XM_024454389.1:c.7976-211_7976-210del XP_024310157.1:n.7976-211_7976-210del
NM_001369.3:c.9374-211_9374-210del MANE Select NP_001360.1:n.9374-211_9374-210del