Canonical Allele Identifier: CA3202988

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13807611T>C , CM000667.2:g.13807611T>C	GRCh38
NC_000005.9:g.13807720T>C , CM000667.1:g.13807720T>C	GRCh37
NC_000005.8:g.13860720T>C	NCBI36
NG_013081.1:g.141870A>G
NG_013081.2:g.141870A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.7867A>G MANE Select	NP_001360.1:p.Thr2623Ala
ENST00000265104.5:c.7867A>G MANE Select	ENSP00000265104.4:p.Thr2623Ala
NM_001369.2:c.7867A>G	NP_001360.1:p.Thr2623Ala
ENST00000265104.4:c.7867A>G	ENSP00000265104.4:p.Thr2623Ala
ENST00000681290.1:c.7822A>G	ENSP00000505288.1:p.Thr2608Ala
XM_005248262.2:c.7822A>G	XP_005248319.1:p.Thr2608Ala
XM_005248262.3:c.7975A>G	XP_005248319.2:p.Thr2659Ala
XM_011513990.1:c.7867A>G	XP_011512292.1:p.Thr2623Ala
XM_017009177.1:c.7975A>G	XP_016864666.1:p.Thr2659Ala
XM_017009178.1:c.6880A>G	XP_016864667.1:p.Thr2294Ala
XM_017009179.2:c.6880A>G	XP_016864668.1:p.Thr2294Ala
XM_017009180.1:c.7975A>G	XP_016864669.1:p.Thr2659Ala
XM_017009181.1:c.7975A>G	XP_016864670.1:p.Thr2659Ala
XM_017009182.1:c.7975A>G	XP_016864671.1:p.Thr2659Ala
XM_017009183.1:c.7975A>G	XP_016864672.1:p.Thr2659Ala
XM_017009184.1:c.7975A>G	XP_016864673.1:p.Thr2659Ala
XM_017009185.1:c.3064A>G	XP_016864674.1:p.Thr1022Ala
XM_017009186.1:c.2617A>G	XP_016864675.1:p.Thr873Ala
XM_017009187.1:c.7975A>G	XP_016864676.1:p.Thr2659Ala
XM_017009188.1:c.1954A>G	XP_016864677.1:p.Thr652Ala
XM_024454388.1:c.6880A>G	XP_024310156.1:p.Thr2294Ala
XM_024454389.1:c.6469A>G	XP_024310157.1:p.Thr2157Ala
XR_001742034.1:n.7992A>G
XR_001742035.1:n.7992A>G
XR_925598.1:n.8074A>G