Canonical Allele Identifier: CA1528431241

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770935T= , CM000667.2:g.13770935T=	GRCh38
NC_000005.9:g.13771044T= , CM000667.1:g.13771044T=	GRCh37
NC_000005.8:g.13824044T=	NCBI36
NG_013081.1:g.178546A=
NG_013081.2:g.178546A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9419A= MANE Select	ENSP00000265104.4:p.Glu3140=
ENST00000681290.1:c.9374A=	ENSP00000505288.1:p.Glu3125=
ENST00000265104.4:c.9419A=	ENSP00000265104.4:p.Glu3140=
ENST00000504001.3:n.131A=
NM_001369.2:c.9419A=	NP_001360.1:p.Glu3140=
XM_005248262.2:c.9374A=	XP_005248319.1:p.Glu3125=
XM_005248262.3:c.9527A=	XP_005248319.2:p.Glu3176=
XM_017009177.1:c.9527A=	XP_016864666.1:p.Glu3176=
XM_017009178.1:c.8432A=	XP_016864667.1:p.Glu2811=
XM_017009179.2:c.8432A=	XP_016864668.1:p.Glu2811=
XM_017009180.1:c.9527A=	XP_016864669.1:p.Glu3176=
XM_017009181.1:c.9527A=	XP_016864670.1:p.Glu3176=
XM_017009182.1:c.9527A=	XP_016864671.1:p.Glu3176=
XM_017009183.1:c.9527A=	XP_016864672.1:p.Glu3176=
XM_017009185.1:c.4616A=	XP_016864674.1:p.Glu1539=
XM_017009186.1:c.4169A=	XP_016864675.1:p.Glu1390=
XM_017009188.1:c.3506A=	XP_016864677.1:p.Glu1169=
XM_024454388.1:c.8432A=	XP_024310156.1:p.Glu2811=
XM_024454389.1:c.8021A=	XP_024310157.1:p.Glu2674=
NM_001369.3:c.9419A= MANE Select	NP_001360.1:p.Glu3140=