Canonical Allele Identifier: CA1528431384
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13771275_13771276delinsAC , CM000667.2:g.13771275_13771276delinsAC GRCh38
NC_000005.9:g.13771384_13771385delinsAC , CM000667.1:g.13771384_13771385delinsAC GRCh37
NC_000005.8:g.13824384_13824385delinsAC NCBI36
NG_013081.1:g.178205_178206delinsGT
NG_013081.2:g.178205_178206delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9374-296_9374-295delinsGT MANE Select ENSP00000265104.4:n.9374-296_9374-295delinsGT
ENST00000681290.1:c.9329-296_9329-295delinsGT ENSP00000505288.1:n.9329-296_9329-295delinsGT
ENST00000265104.4:c.9374-296_9374-295delinsGT ENSP00000265104.4:n.9374-296_9374-295delinsGT
ENST00000504001.3:n.7_8delinsGT
NM_001369.2:c.9374-296_9374-295delinsGT NP_001360.1:n.9374-296_9374-295delinsGT
XM_005248262.2:c.9329-296_9329-295delinsGT XP_005248319.1:n.9329-296_9329-295delinsGT
XM_005248262.3:c.9482-296_9482-295delinsGT XP_005248319.2:n.9482-296_9482-295delinsGT
XM_017009177.1:c.9482-296_9482-295delinsGT XP_016864666.1:n.9482-296_9482-295delinsGT
XM_017009178.1:c.8387-296_8387-295delinsGT XP_016864667.1:n.8387-296_8387-295delinsGT
XM_017009179.2:c.8387-296_8387-295delinsGT XP_016864668.1:n.8387-296_8387-295delinsGT
XM_017009180.1:c.9482-296_9482-295delinsGT XP_016864669.1:n.9482-296_9482-295delinsGT
XM_017009181.1:c.9482-296_9482-295delinsGT XP_016864670.1:n.9482-296_9482-295delinsGT
XM_017009182.1:c.9482-296_9482-295delinsGT XP_016864671.1:n.9482-296_9482-295delinsGT
XM_017009183.1:c.9482-296_9482-295delinsGT XP_016864672.1:n.9482-296_9482-295delinsGT
XM_017009185.1:c.4571-296_4571-295delinsGT XP_016864674.1:n.4571-296_4571-295delinsGT
XM_017009186.1:c.4124-296_4124-295delinsGT XP_016864675.1:n.4124-296_4124-295delinsGT
XM_017009188.1:c.3461-296_3461-295delinsGT XP_016864677.1:n.3461-296_3461-295delinsGT
XM_024454388.1:c.8387-296_8387-295delinsGT XP_024310156.1:n.8387-296_8387-295delinsGT
XM_024454389.1:c.7976-296_7976-295delinsGT XP_024310157.1:n.7976-296_7976-295delinsGT
NM_001369.3:c.9374-296_9374-295delinsGT MANE Select NP_001360.1:n.9374-296_9374-295delinsGT