Canonical Allele Identifier: CA1528431236
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13770922C= , CM000667.2:g.13770922C= GRCh38
NC_000005.9:g.13771031C= , CM000667.1:g.13771031C= GRCh37
NC_000005.8:g.13824031C= NCBI36
NG_013081.1:g.178559G=
NG_013081.2:g.178559G=

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.9432G= MANE Select ENSP00000265104.4:p.Glu3144=
ENST00000681290.1:c.9387G= ENSP00000505288.1:p.Glu3129=
ENST00000265104.4:c.9432G= ENSP00000265104.4:p.Glu3144=
ENST00000504001.3:n.144G=
NM_001369.2:c.9432G= NP_001360.1:p.Glu3144=
XM_005248262.2:c.9387G= XP_005248319.1:p.Glu3129=
XM_005248262.3:c.9540G= XP_005248319.2:p.Glu3180=
XM_017009177.1:c.9540G= XP_016864666.1:p.Glu3180=
XM_017009178.1:c.8445G= XP_016864667.1:p.Glu2815=
XM_017009179.2:c.8445G= XP_016864668.1:p.Glu2815=
XM_017009180.1:c.9540G= XP_016864669.1:p.Glu3180=
XM_017009181.1:c.9540G= XP_016864670.1:p.Glu3180=
XM_017009182.1:c.9540G= XP_016864671.1:p.Glu3180=
XM_017009183.1:c.9540G= XP_016864672.1:p.Glu3180=
XM_017009185.1:c.4629G= XP_016864674.1:p.Glu1543=
XM_017009186.1:c.4182G= XP_016864675.1:p.Glu1394=
XM_017009188.1:c.3519G= XP_016864677.1:p.Glu1173=
XM_024454388.1:c.8445G= XP_024310156.1:p.Glu2815=
XM_024454389.1:c.8034G= XP_024310157.1:p.Glu2678=
NM_001369.3:c.9432G= MANE Select NP_001360.1:p.Glu3144=