Canonical Allele Identifier: CA359189704
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13752154T>G , CM000667.2:g.13752154T>G GRCh38
NC_000005.9:g.13752263T>G , CM000667.1:g.13752263T>G GRCh37
NC_000005.8:g.13805263T>G NCBI36
NG_013081.1:g.197327A>C
NG_013081.2:g.197327A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.11008A>C MANE Select ENSP00000265104.4:p.Lys3670Gln
ENST00000681290.1:c.10963A>C ENSP00000505288.1:p.Lys3655Gln
ENST00000265104.4:c.11008A>C ENSP00000265104.4:p.Lys3670Gln
NM_001369.2:c.11008A>C NP_001360.1:p.Lys3670Gln
XM_005248262.2:c.10963A>C XP_005248319.1:p.Lys3655Gln
XM_005248262.3:c.11116A>C XP_005248319.2:p.Lys3706Gln
XM_017009177.1:c.11116A>C XP_016864666.1:p.Lys3706Gln
XM_017009178.1:c.10021A>C XP_016864667.1:p.Lys3341Gln
XM_017009179.2:c.10021A>C XP_016864668.1:p.Lys3341Gln
XM_017009180.1:c.11116A>C XP_016864669.1:p.Lys3706Gln
XM_017009181.1:c.11116A>C XP_016864670.1:p.Lys3706Gln
XM_017009182.1:c.11116A>C XP_016864671.1:p.Lys3706Gln
XM_017009185.1:c.6205A>C XP_016864674.1:p.Lys2069Gln
XM_017009186.1:c.5758A>C XP_016864675.1:p.Lys1920Gln
XM_017009188.1:c.5095A>C XP_016864677.1:p.Lys1699Gln
XM_024454388.1:c.10021A>C XP_024310156.1:p.Lys3341Gln
XM_024454389.1:c.9610A>C XP_024310157.1:p.Lys3204Gln
NM_001369.3:c.11008A>C MANE Select NP_001360.1:p.Lys3670Gln