Canonical Allele Identifier: CA1528431160

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770735A= , CM000667.2:g.13770735A=	GRCh38
NC_000005.9:g.13770844A= , CM000667.1:g.13770844A=	GRCh37
NC_000005.8:g.13823844A=	NCBI36
NG_013081.1:g.178746T=
NG_013081.2:g.178746T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9605+14T= MANE Select	ENSP00000265104.4:n.9605+14T=
ENST00000681290.1:c.9560+14T=	ENSP00000505288.1:n.9560+14T=
ENST00000265104.4:c.9605+14T=	ENSP00000265104.4:n.9605+14T=
ENST00000504001.3:n.317+14T=
NM_001369.2:c.9605+14T=	NP_001360.1:n.9605+14T=
XM_005248262.2:c.9560+14T=	XP_005248319.1:n.9560+14T=
XM_005248262.3:c.9713+14T=	XP_005248319.2:n.9713+14T=
XM_017009177.1:c.9713+14T=	XP_016864666.1:n.9713+14T=
XM_017009178.1:c.8618+14T=	XP_016864667.1:n.8618+14T=
XM_017009179.2:c.8618+14T=	XP_016864668.1:n.8618+14T=
XM_017009180.1:c.9713+14T=	XP_016864669.1:n.9713+14T=
XM_017009181.1:c.9713+14T=	XP_016864670.1:n.9713+14T=
XM_017009182.1:c.9713+14T=	XP_016864671.1:n.9713+14T=
XM_017009183.1:c.*10T=	XP_016864672.1:n.*10T=
XM_017009185.1:c.4802+14T=	XP_016864674.1:n.4802+14T=
XM_017009186.1:c.4355+14T=	XP_016864675.1:n.4355+14T=
XM_017009188.1:c.3692+14T=	XP_016864677.1:n.3692+14T=
XM_024454388.1:c.8618+14T=	XP_024310156.1:n.8618+14T=
XM_024454389.1:c.8207+14T=	XP_024310157.1:n.8207+14T=
NM_001369.3:c.9605+14T= MANE Select	NP_001360.1:n.9605+14T=