Canonical Allele Identifier: CA3202380

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13766165C>T , CM000667.2:g.13766165C>T	GRCh38
NC_000005.9:g.13766274C>T , CM000667.1:g.13766274C>T	GRCh37
NC_000005.8:g.13819274C>T	NCBI36
NG_013081.1:g.183316G>A
NG_013081.2:g.183316G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.9912G>A MANE Select	NP_001360.1:p.Ser3304=
ENST00000265104.5:c.9912G>A MANE Select	ENSP00000265104.4:p.Ser3304=
NM_001369.2:c.9912G>A	NP_001360.1:p.Ser3304=
ENST00000265104.4:c.9912G>A	ENSP00000265104.4:p.Ser3304=
ENST00000504001.3:n.609+2795G>A
ENST00000681290.1:c.9867G>A	ENSP00000505288.1:p.Ser3289=
XM_005248262.2:c.9867G>A	XP_005248319.1:p.Ser3289=
XM_005248262.3:c.10020G>A	XP_005248319.2:p.Ser3340=
XM_017009177.1:c.10020G>A	XP_016864666.1:p.Ser3340=
XM_017009178.1:c.8925G>A	XP_016864667.1:p.Ser2975=
XM_017009179.2:c.8925G>A	XP_016864668.1:p.Ser2975=
XM_017009180.1:c.10020G>A	XP_016864669.1:p.Ser3340=
XM_017009181.1:c.10020G>A	XP_016864670.1:p.Ser3340=
XM_017009182.1:c.10020G>A	XP_016864671.1:p.Ser3340=
XM_017009185.1:c.5109G>A	XP_016864674.1:p.Ser1703=
XM_017009186.1:c.4662G>A	XP_016864675.1:p.Ser1554=
XM_017009188.1:c.3999G>A	XP_016864677.1:p.Ser1333=
XM_024454388.1:c.8925G>A	XP_024310156.1:p.Ser2975=
XM_024454389.1:c.8514G>A	XP_024310157.1:p.Ser2838=