Canonical Allele Identifier: CA443272352

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13809062G>A , CM000667.2:g.13809062G>A	GRCh38
NC_000005.9:g.13809171G>A , CM000667.1:g.13809171G>A	GRCh37
NC_000005.8:g.13862171G>A	NCBI36
NG_013081.1:g.140419C>T
NG_013081.2:g.140419C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.7734C>T MANE Select	NP_001360.1:p.Thr2578=
ENST00000265104.5:c.7734C>T MANE Select	ENSP00000265104.4:p.Thr2578=
NM_001369.2:c.7734C>T	NP_001360.1:p.Thr2578=
ENST00000265104.4:c.7734C>T	ENSP00000265104.4:p.Thr2578=
ENST00000512443.1:n.590C>T
ENST00000681290.1:c.7689C>T	ENSP00000505288.1:p.Thr2563=
XM_005248262.2:c.7689C>T	XP_005248319.1:p.Thr2563=
XM_005248262.3:c.7842C>T	XP_005248319.2:p.Thr2614=
XM_011513990.1:c.7734C>T	XP_011512292.1:p.Thr2578=
XM_017009177.1:c.7842C>T	XP_016864666.1:p.Thr2614=
XM_017009178.1:c.6747C>T	XP_016864667.1:p.Thr2249=
XM_017009179.2:c.6747C>T	XP_016864668.1:p.Thr2249=
XM_017009180.1:c.7842C>T	XP_016864669.1:p.Thr2614=
XM_017009181.1:c.7842C>T	XP_016864670.1:p.Thr2614=
XM_017009182.1:c.7842C>T	XP_016864671.1:p.Thr2614=
XM_017009183.1:c.7842C>T	XP_016864672.1:p.Thr2614=
XM_017009184.1:c.7842C>T	XP_016864673.1:p.Thr2614=
XM_017009185.1:c.2931C>T	XP_016864674.1:p.Thr977=
XM_017009186.1:c.2484C>T	XP_016864675.1:p.Thr828=
XM_017009187.1:c.7842C>T	XP_016864676.1:p.Thr2614=
XM_017009188.1:c.1821C>T	XP_016864677.1:p.Thr607=
XM_024454388.1:c.6747C>T	XP_024310156.1:p.Thr2249=
XM_024454389.1:c.6336C>T	XP_024310157.1:p.Thr2112=
XR_001742034.1:n.7859C>T
XR_001742035.1:n.7859C>T
XR_925598.1:n.7941C>T