Canonical Allele Identifier: CA1073401921
Gene: DNAH5 HGNC NCBI

Linked Data

dbSNP Id: rs1750562798

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13753565_13753568del , CM000667.2:g.13753565_13753568del GRCh38
NC_000005.9:g.13753674_13753677del , CM000667.1:g.13753674_13753677del GRCh37
NC_000005.8:g.13806674_13806677del NCBI36
NG_013081.1:g.195918_195921del
NG_013081.2:g.195918_195921del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.10556-14_10556-11del MANE Select ENSP00000265104.4:n.10556-14_10556-11del
ENST00000681290.1:c.10511-14_10511-11del ENSP00000505288.1:n.10511-14_10511-11del
ENST00000265104.4:c.10556-14_10556-11del ENSP00000265104.4:n.10556-14_10556-11del
NM_001369.2:c.10556-14_10556-11del NP_001360.1:n.10556-14_10556-11del
XM_005248262.2:c.10511-14_10511-11del XP_005248319.1:n.10511-14_10511-11del
XM_005248262.3:c.10664-14_10664-11del XP_005248319.2:n.10664-14_10664-11del
XM_017009177.1:c.10664-14_10664-11del XP_016864666.1:n.10664-14_10664-11del
XM_017009178.1:c.9569-14_9569-11del XP_016864667.1:n.9569-14_9569-11del
XM_017009179.2:c.9569-14_9569-11del XP_016864668.1:n.9569-14_9569-11del
XM_017009180.1:c.10664-14_10664-11del XP_016864669.1:n.10664-14_10664-11del
XM_017009181.1:c.10664-14_10664-11del XP_016864670.1:n.10664-14_10664-11del
XM_017009182.1:c.10664-14_10664-11del XP_016864671.1:n.10664-14_10664-11del
XM_017009185.1:c.5753-14_5753-11del XP_016864674.1:n.5753-14_5753-11del
XM_017009186.1:c.5306-14_5306-11del XP_016864675.1:n.5306-14_5306-11del
XM_017009188.1:c.4643-14_4643-11del XP_016864677.1:n.4643-14_4643-11del
XM_024454388.1:c.9569-14_9569-11del XP_024310156.1:n.9569-14_9569-11del
XM_024454389.1:c.9158-14_9158-11del XP_024310157.1:n.9158-14_9158-11del
NM_001369.3:c.10556-14_10556-11del MANE Select NP_001360.1:n.10556-14_10556-11del