Canonical Allele Identifier: CA1528498266

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13919050G= , CM000667.2:g.13919050G=	GRCh38
NC_000005.9:g.13919159G= , CM000667.1:g.13919159G=	GRCh37
NC_000005.8:g.13972159G=	NCBI36
NG_013081.1:g.30431C=
NG_013081.2:g.30431C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000680213.2:n.1031+126C=
ENST00000682376.1:n.1145C=
ENST00000682586.1:n.1194C=
ENST00000683011.1:n.914+126C=
ENST00000683967.1:n.1074+126C=
ENST00000684013.1:n.1074+126C=
ENST00000684099.1:n.1070+126C=
ENST00000265104.5:c.975+126C= MANE Select	ENSP00000265104.4:n.975+126C=
ENST00000680213.1:c.735+126C=	ENSP00000506622.1:n.735+126C=
ENST00000681290.1:c.930+126C=	ENSP00000505288.1:n.930+126C=
ENST00000265104.4:c.975+126C=	ENSP00000265104.4:n.975+126C=
ENST00000508040.1:n.1383+126C=
NM_001369.2:c.975+126C=	NP_001360.1:n.975+126C=
XM_005248262.2:c.930+126C=	XP_005248319.1:n.930+126C=
XM_011513990.1:c.975+126C=	XP_011512292.1:n.975+126C=
XR_925598.1:n.1182+126C=
XM_005248262.3:c.1083+126C=	XP_005248319.2:n.1083+126C=
XM_017009177.1:c.1083+126C=	XP_016864666.1:n.1083+126C=
XM_017009178.1:c.-13+126C=	XP_016864667.1:n.-13+126C=
XM_017009179.2:c.-90C=	XP_016864668.1:n.-90C=
XM_017009180.1:c.1083+126C=	XP_016864669.1:n.1083+126C=
XM_017009181.1:c.1083+126C=	XP_016864670.1:n.1083+126C=
XM_017009182.1:c.1083+126C=	XP_016864671.1:n.1083+126C=
XM_017009183.1:c.1083+126C=	XP_016864672.1:n.1083+126C=
XM_017009184.1:c.1083+126C=	XP_016864673.1:n.1083+126C=
XM_017009187.1:c.1083+126C=	XP_016864676.1:n.1083+126C=
XM_024454388.1:c.-1806C=	XP_024310156.1:n.-1806C=
XM_024454389.1:c.-985+126C=	XP_024310157.1:n.-985+126C=
XR_001742034.1:n.1100+126C=
XR_001742035.1:n.1100+126C=
NM_001369.3:c.975+126C= MANE Select	NP_001360.1:n.975+126C=