Canonical Allele Identifier: CA1528435099

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776506G= , CM000667.2:g.13776506G=	GRCh38
NC_000005.9:g.13776615G= , CM000667.1:g.13776615G=	GRCh37
NC_000005.8:g.13829615G=	NCBI36
NG_013081.1:g.172975C=
NG_013081.2:g.172975C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9306C= MANE Select	ENSP00000265104.4:p.Phe3102=
ENST00000681290.1:c.9261C=	ENSP00000505288.1:p.Phe3087=
ENST00000265104.4:c.9306C=	ENSP00000265104.4:p.Phe3102=
NM_001369.2:c.9306C=	NP_001360.1:p.Phe3102=
XM_005248262.2:c.9261C=	XP_005248319.1:p.Phe3087=
XM_005248262.3:c.9414C=	XP_005248319.2:p.Phe3138=
XM_017009177.1:c.9414C=	XP_016864666.1:p.Phe3138=
XM_017009178.1:c.8319C=	XP_016864667.1:p.Phe2773=
XM_017009179.2:c.8319C=	XP_016864668.1:p.Phe2773=
XM_017009180.1:c.9414C=	XP_016864669.1:p.Phe3138=
XM_017009181.1:c.9414C=	XP_016864670.1:p.Phe3138=
XM_017009182.1:c.9414C=	XP_016864671.1:p.Phe3138=
XM_017009183.1:c.9414C=	XP_016864672.1:p.Phe3138=
XM_017009185.1:c.4503C=	XP_016864674.1:p.Phe1501=
XM_017009186.1:c.4056C=	XP_016864675.1:p.Phe1352=
XM_017009188.1:c.3393C=	XP_016864677.1:p.Phe1131=
XM_024454388.1:c.8319C=	XP_024310156.1:p.Phe2773=
XM_024454389.1:c.7908C=	XP_024310157.1:p.Phe2636=
NM_001369.3:c.9306C= MANE Select	NP_001360.1:p.Phe3102=