Canonical Allele Identifier: CA1528399807
Gene: DNAH5 HGNC NCBI

Linked Data

dbSNP Id: rs1742050303

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13701130_13701132del , CM000667.2:g.13701130_13701132del GRCh38
NC_000005.9:g.13701239_13701241del , CM000667.1:g.13701239_13701241del GRCh37
NC_000005.8:g.13754239_13754241del NCBI36
NG_013081.1:g.248352_248354del
NG_013081.2:g.248352_248354del

Transcript Alleles

HGVS Amino-acid Change
ENST00000683611.1:n.824+155_824+157del
ENST00000265104.5:c.13491+155_13491+157del MANE Select ENSP00000265104.4:n.13491+155_13491+157del
ENST00000681290.1:c.13446+155_13446+157del ENSP00000505288.1:n.13446+155_13446+157del
ENST00000265104.4:c.13491+155_13491+157del ENSP00000265104.4:n.13491+155_13491+157del
NM_001369.2:c.13491+155_13491+157del NP_001360.1:n.13491+155_13491+157del
XM_005248262.2:c.13446+155_13446+157del XP_005248319.1:n.13446+155_13446+157del
XM_005248262.3:c.13599+155_13599+157del XP_005248319.2:n.13599+155_13599+157del
XM_017009177.1:c.13179+155_13179+157del XP_016864666.1:n.13179+155_13179+157del
XM_017009178.1:c.12504+155_12504+157del XP_016864667.1:n.12504+155_12504+157del
XM_017009179.2:c.12504+155_12504+157del XP_016864668.1:n.12504+155_12504+157del
XM_017009185.1:c.8688+155_8688+157del XP_016864674.1:n.8688+155_8688+157del
XM_017009186.1:c.8241+155_8241+157del XP_016864675.1:n.8241+155_8241+157del
XM_017009188.1:c.7578+155_7578+157del XP_016864677.1:n.7578+155_7578+157del
XM_024454388.1:c.12504+155_12504+157del XP_024310156.1:n.12504+155_12504+157del
XM_024454389.1:c.12093+155_12093+157del XP_024310157.1:n.12093+155_12093+157del
NM_001369.3:c.13491+155_13491+157del MANE Select NP_001360.1:n.13491+155_13491+157del