Canonical Allele Identifier: CA2521046601
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13771303_13771304insAG , CM000667.2:g.13771303_13771304insAG GRCh38
NC_000005.9:g.13771412_13771413insAG , CM000667.1:g.13771412_13771413insAG GRCh37
NC_000005.8:g.13824412_13824413insAG NCBI36
NG_013081.1:g.178177_178178insCT
NG_013081.2:g.178177_178178insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9374-324_9374-323insCT MANE Select ENSP00000265104.4:n.9374-324_9374-323insCT
ENST00000681290.1:c.9329-324_9329-323insCT ENSP00000505288.1:n.9329-324_9329-323insCT
ENST00000265104.4:c.9374-324_9374-323insCT ENSP00000265104.4:n.9374-324_9374-323insCT
NM_001369.2:c.9374-324_9374-323insCT NP_001360.1:n.9374-324_9374-323insCT
XM_005248262.2:c.9329-324_9329-323insCT XP_005248319.1:n.9329-324_9329-323insCT
XM_005248262.3:c.9482-324_9482-323insCT XP_005248319.2:n.9482-324_9482-323insCT
XM_017009177.1:c.9482-324_9482-323insCT XP_016864666.1:n.9482-324_9482-323insCT
XM_017009178.1:c.8387-324_8387-323insCT XP_016864667.1:n.8387-324_8387-323insCT
XM_017009179.2:c.8387-324_8387-323insCT XP_016864668.1:n.8387-324_8387-323insCT
XM_017009180.1:c.9482-324_9482-323insCT XP_016864669.1:n.9482-324_9482-323insCT
XM_017009181.1:c.9482-324_9482-323insCT XP_016864670.1:n.9482-324_9482-323insCT
XM_017009182.1:c.9482-324_9482-323insCT XP_016864671.1:n.9482-324_9482-323insCT
XM_017009183.1:c.9482-324_9482-323insCT XP_016864672.1:n.9482-324_9482-323insCT
XM_017009185.1:c.4571-324_4571-323insCT XP_016864674.1:n.4571-324_4571-323insCT
XM_017009186.1:c.4124-324_4124-323insCT XP_016864675.1:n.4124-324_4124-323insCT
XM_017009188.1:c.3461-324_3461-323insCT XP_016864677.1:n.3461-324_3461-323insCT
XM_024454388.1:c.8387-324_8387-323insCT XP_024310156.1:n.8387-324_8387-323insCT
XM_024454389.1:c.7976-324_7976-323insCT XP_024310157.1:n.7976-324_7976-323insCT
NM_001369.3:c.9374-324_9374-323insCT MANE Select NP_001360.1:n.9374-324_9374-323insCT