Canonical Allele Identifier: CA3123573762

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13919319C= , CM000667.2:g.13919319C=	GRCh38
NC_000005.9:g.13919428C= , CM000667.1:g.13919428C=	GRCh37
NC_000005.8:g.13972428C=	NCBI36
NG_013081.1:g.30162G=
NG_013081.2:g.30162G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000680213.2:n.888G=
ENST00000682376.1:n.876G=
ENST00000682586.1:n.925G=
ENST00000683011.1:n.771G=
ENST00000683967.1:n.931G=
ENST00000684013.1:n.931G=
ENST00000684099.1:n.927G=
ENST00000265104.5:c.832G= MANE Select	ENSP00000265104.4:p.Ala278=
ENST00000680213.1:c.592G=	ENSP00000506622.1:p.Ala198=
ENST00000681290.1:c.787G=	ENSP00000505288.1:p.Ala263=
ENST00000265104.4:c.832G=	ENSP00000265104.4:p.Ala278=
ENST00000508040.1:n.1240G=
NM_001369.2:c.832G=	NP_001360.1:p.Ala278=
XM_005248262.2:c.787G=	XP_005248319.1:p.Ala263=
XM_011513990.1:c.832G=	XP_011512292.1:p.Ala278=
XR_925598.1:n.1039G=
XM_005248262.3:c.940G=	XP_005248319.2:p.Ala314=
XM_017009177.1:c.940G=	XP_016864666.1:p.Ala314=
XM_017009178.1:c.-156G=	XP_016864667.1:n.-156G=
XM_017009180.1:c.940G=	XP_016864669.1:p.Ala314=
XM_017009181.1:c.940G=	XP_016864670.1:p.Ala314=
XM_017009182.1:c.940G=	XP_016864671.1:p.Ala314=
XM_017009183.1:c.940G=	XP_016864672.1:p.Ala314=
XM_017009184.1:c.940G=	XP_016864673.1:p.Ala314=
XM_017009187.1:c.940G=	XP_016864676.1:p.Ala314=
XM_024454388.1:c.-2075G=	XP_024310156.1:n.-2075G=
XM_024454389.1:c.-1128G=	XP_024310157.1:n.-1128G=
XR_001742034.1:n.957G=
XR_001742035.1:n.957G=
NM_001369.3:c.832G= MANE Select	NP_001360.1:p.Ala278=