Canonical Allele Identifier: CA359191653
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13753398A>C , CM000667.2:g.13753398A>C GRCh38
NC_000005.9:g.13753507A>C , CM000667.1:g.13753507A>C GRCh37
NC_000005.8:g.13806507A>C NCBI36
NG_013081.1:g.196083T>G
NG_013081.2:g.196083T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.10707T>G MANE Select ENSP00000265104.4:p.Asp3569Glu
ENST00000681290.1:c.10662T>G ENSP00000505288.1:p.Asp3554Glu
ENST00000265104.4:c.10707T>G ENSP00000265104.4:p.Asp3569Glu
NM_001369.2:c.10707T>G NP_001360.1:p.Asp3569Glu
XM_005248262.2:c.10662T>G XP_005248319.1:p.Asp3554Glu
XM_005248262.3:c.10815T>G XP_005248319.2:p.Asp3605Glu
XM_017009177.1:c.10815T>G XP_016864666.1:p.Asp3605Glu
XM_017009178.1:c.9720T>G XP_016864667.1:p.Asp3240Glu
XM_017009179.2:c.9720T>G XP_016864668.1:p.Asp3240Glu
XM_017009180.1:c.10815T>G XP_016864669.1:p.Asp3605Glu
XM_017009181.1:c.10815T>G XP_016864670.1:p.Asp3605Glu
XM_017009182.1:c.10815T>G XP_016864671.1:p.Asp3605Glu
XM_017009185.1:c.5904T>G XP_016864674.1:p.Asp1968Glu
XM_017009186.1:c.5457T>G XP_016864675.1:p.Asp1819Glu
XM_017009188.1:c.4794T>G XP_016864677.1:p.Asp1598Glu
XM_024454388.1:c.9720T>G XP_024310156.1:p.Asp3240Glu
XM_024454389.1:c.9309T>G XP_024310157.1:p.Asp3103Glu
NM_001369.3:c.10707T>G MANE Select NP_001360.1:p.Asp3569Glu