Canonical Allele Identifier: CA2708139069
Gene: DNAH5 HGNC NCBI

Linked Data

dbSNP Id: rs2126328777

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13691704_13691706del , CM000667.2:g.13691704_13691706del GRCh38
NC_000005.9:g.13691813_13691815del , CM000667.1:g.13691813_13691815del GRCh37
NC_000005.8:g.13744813_13744815del NCBI36
NG_013081.1:g.257780_257782del
NG_013081.2:g.257780_257782del

Transcript Alleles

HGVS Amino-acid Change
ENST00000683611.1:n.1491_1493del
ENST00000265104.5:c.*283_*285del MANE Select ENSP00000265104.4:n.*283_*285del
ENST00000681290.1:c.*283_*285del ENSP00000505288.1:n.*283_*285del
ENST00000265104.4:c.*283_*285del ENSP00000265104.4:n.*283_*285del
NM_001369.2:c.*283_*285del NP_001360.1:n.*283_*285del
XM_005248262.2:c.*283_*285del XP_005248319.1:n.*283_*285del
XM_005248262.3:c.*283_*285del XP_005248319.2:n.*283_*285del
XM_017009177.1:c.*283_*285del XP_016864666.1:n.*283_*285del
XM_017009178.1:c.*283_*285del XP_016864667.1:n.*283_*285del
XM_017009179.2:c.*283_*285del XP_016864668.1:n.*283_*285del
XM_017009185.1:c.*283_*285del XP_016864674.1:n.*283_*285del
XM_017009186.1:c.*283_*285del XP_016864675.1:n.*283_*285del
XM_017009188.1:c.*283_*285del XP_016864677.1:n.*283_*285del
XM_024454388.1:c.*283_*285del XP_024310156.1:n.*283_*285del
XM_024454389.1:c.*283_*285del XP_024310157.1:n.*283_*285del
NM_001369.3:c.*283_*285del MANE Select NP_001360.1:n.*283_*285del