Canonical Allele Identifier: CA1528431335
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13771146_13771147delinsTC , CM000667.2:g.13771146_13771147delinsTC GRCh38
NC_000005.9:g.13771255_13771256delinsTC , CM000667.1:g.13771255_13771256delinsTC GRCh37
NC_000005.8:g.13824255_13824256delinsTC NCBI36
NG_013081.1:g.178334_178335delinsGA
NG_013081.2:g.178334_178335delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9374-167_9374-166delinsGA MANE Select ENSP00000265104.4:n.9374-167_9374-166delinsGA
ENST00000681290.1:c.9329-167_9329-166delinsGA ENSP00000505288.1:n.9329-167_9329-166delinsGA
ENST00000265104.4:c.9374-167_9374-166delinsGA ENSP00000265104.4:n.9374-167_9374-166delinsGA
ENST00000504001.3:n.85+51_85+52delinsGA
NM_001369.2:c.9374-167_9374-166delinsGA NP_001360.1:n.9374-167_9374-166delinsGA
XM_005248262.2:c.9329-167_9329-166delinsGA XP_005248319.1:n.9329-167_9329-166delinsGA
XM_005248262.3:c.9482-167_9482-166delinsGA XP_005248319.2:n.9482-167_9482-166delinsGA
XM_017009177.1:c.9482-167_9482-166delinsGA XP_016864666.1:n.9482-167_9482-166delinsGA
XM_017009178.1:c.8387-167_8387-166delinsGA XP_016864667.1:n.8387-167_8387-166delinsGA
XM_017009179.2:c.8387-167_8387-166delinsGA XP_016864668.1:n.8387-167_8387-166delinsGA
XM_017009180.1:c.9482-167_9482-166delinsGA XP_016864669.1:n.9482-167_9482-166delinsGA
XM_017009181.1:c.9482-167_9482-166delinsGA XP_016864670.1:n.9482-167_9482-166delinsGA
XM_017009182.1:c.9482-167_9482-166delinsGA XP_016864671.1:n.9482-167_9482-166delinsGA
XM_017009183.1:c.9482-167_9482-166delinsGA XP_016864672.1:n.9482-167_9482-166delinsGA
XM_017009185.1:c.4571-167_4571-166delinsGA XP_016864674.1:n.4571-167_4571-166delinsGA
XM_017009186.1:c.4124-167_4124-166delinsGA XP_016864675.1:n.4124-167_4124-166delinsGA
XM_017009188.1:c.3461-167_3461-166delinsGA XP_016864677.1:n.3461-167_3461-166delinsGA
XM_024454388.1:c.8387-167_8387-166delinsGA XP_024310156.1:n.8387-167_8387-166delinsGA
XM_024454389.1:c.7976-167_7976-166delinsGA XP_024310157.1:n.7976-167_7976-166delinsGA
NM_001369.3:c.9374-167_9374-166delinsGA MANE Select NP_001360.1:n.9374-167_9374-166delinsGA