Canonical Allele Identifier: CA1528430363

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13769042C= , CM000667.2:g.13769042C=	GRCh38
NC_000005.9:g.13769151C= , CM000667.1:g.13769151C=	GRCh37
NC_000005.8:g.13822151C=	NCBI36
NG_013081.1:g.180439G=
NG_013081.2:g.180439G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9815G= MANE Select	ENSP00000265104.4:p.Ser3272=
ENST00000681290.1:c.9770G=	ENSP00000505288.1:p.Ser3257=
ENST00000265104.4:c.9815G=	ENSP00000265104.4:p.Ser3272=
ENST00000504001.3:n.527G=
NM_001369.2:c.9815G=	NP_001360.1:p.Ser3272=
XM_005248262.2:c.9770G=	XP_005248319.1:p.Ser3257=
XM_005248262.3:c.9923G=	XP_005248319.2:p.Ser3308=
XM_017009177.1:c.9923G=	XP_016864666.1:p.Ser3308=
XM_017009178.1:c.8828G=	XP_016864667.1:p.Ser2943=
XM_017009179.2:c.8828G=	XP_016864668.1:p.Ser2943=
XM_017009180.1:c.9923G=	XP_016864669.1:p.Ser3308=
XM_017009181.1:c.9923G=	XP_016864670.1:p.Ser3308=
XM_017009182.1:c.9923G=	XP_016864671.1:p.Ser3308=
XM_017009185.1:c.5012G=	XP_016864674.1:p.Ser1671=
XM_017009186.1:c.4565G=	XP_016864675.1:p.Ser1522=
XM_017009188.1:c.3902G=	XP_016864677.1:p.Ser1301=
XM_024454388.1:c.8828G=	XP_024310156.1:p.Ser2943=
XM_024454389.1:c.8417G=	XP_024310157.1:p.Ser2806=
NM_001369.3:c.9815G= MANE Select	NP_001360.1:p.Ser3272=