Canonical Allele Identifier: CA1528407078

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13717500C= , CM000667.2:g.13717500C=	GRCh38
NC_000005.9:g.13717609C= , CM000667.1:g.13717609C=	GRCh37
NC_000005.8:g.13770609C=	NCBI36
NG_013081.1:g.231981G=
NG_013081.2:g.231981G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.12520G= MANE Select	ENSP00000265104.4:p.Asp4174=
ENST00000681290.1:c.12475G=	ENSP00000505288.1:p.Asp4159=
ENST00000265104.4:c.12520G=	ENSP00000265104.4:p.Asp4174=
NM_001369.2:c.12520G=	NP_001360.1:p.Asp4174=
XM_005248262.2:c.12475G=	XP_005248319.1:p.Asp4159=
XM_005248262.3:c.12628G=	XP_005248319.2:p.Asp4210=
XM_017009177.1:c.12628G=	XP_016864666.1:p.Asp4210=
XM_017009178.1:c.11533G=	XP_016864667.1:p.Asp3845=
XM_017009179.2:c.11533G=	XP_016864668.1:p.Asp3845=
XM_017009180.1:c.12628G=	XP_016864669.1:p.Asp4210=
XM_017009185.1:c.7717G=	XP_016864674.1:p.Asp2573=
XM_017009186.1:c.7270G=	XP_016864675.1:p.Asp2424=
XM_017009188.1:c.6607G=	XP_016864677.1:p.Asp2203=
XM_024454388.1:c.11533G=	XP_024310156.1:p.Asp3845=
XM_024454389.1:c.11122G=	XP_024310157.1:p.Asp3708=
NM_001369.3:c.12520G= MANE Select	NP_001360.1:p.Asp4174=