Canonical Allele Identifier: CA3202745

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13786235G>A , CM000667.2:g.13786235G>A	GRCh38
NC_000005.9:g.13786344G>A , CM000667.1:g.13786344G>A	GRCh37
NC_000005.8:g.13839344G>A	NCBI36
NG_013081.1:g.163246C>T
NG_013081.2:g.163246C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.8764C>T MANE Select	NP_001360.1:p.Arg2922Cys
ENST00000265104.5:c.8764C>T MANE Select	ENSP00000265104.4:p.Arg2922Cys
NM_001369.2:c.8764C>T	NP_001360.1:p.Arg2922Cys
ENST00000265104.4:c.8764C>T	ENSP00000265104.4:p.Arg2922Cys
ENST00000681290.1:c.8719C>T	ENSP00000505288.1:p.Arg2907Cys
XM_005248262.2:c.8719C>T	XP_005248319.1:p.Arg2907Cys
XM_005248262.3:c.8872C>T	XP_005248319.2:p.Arg2958Cys
XM_011513990.1:c.8764C>T	XP_011512292.1:p.Arg2922Cys
XM_017009177.1:c.8872C>T	XP_016864666.1:p.Arg2958Cys
XM_017009178.1:c.7777C>T	XP_016864667.1:p.Arg2593Cys
XM_017009179.2:c.7777C>T	XP_016864668.1:p.Arg2593Cys
XM_017009180.1:c.8872C>T	XP_016864669.1:p.Arg2958Cys
XM_017009181.1:c.8872C>T	XP_016864670.1:p.Arg2958Cys
XM_017009182.1:c.8872C>T	XP_016864671.1:p.Arg2958Cys
XM_017009183.1:c.8872C>T	XP_016864672.1:p.Arg2958Cys
XM_017009184.1:c.8872C>T	XP_016864673.1:p.Arg2958Cys
XM_017009185.1:c.3961C>T	XP_016864674.1:p.Arg1321Cys
XM_017009186.1:c.3514C>T	XP_016864675.1:p.Arg1172Cys
XM_017009188.1:c.2851C>T	XP_016864677.1:p.Arg951Cys
XM_024454388.1:c.7777C>T	XP_024310156.1:p.Arg2593Cys
XM_024454389.1:c.7366C>T	XP_024310157.1:p.Arg2456Cys
XR_001742034.1:n.8889C>T
XR_001742035.1:n.8889C>T
XR_925598.1:n.8971C>T