Canonical Allele Identifier: CA1528415141

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735935G= , CM000667.2:g.13735935G=	GRCh38
NC_000005.9:g.13736044G= , CM000667.1:g.13736044G=	GRCh37
NC_000005.8:g.13789044G=	NCBI36
NG_013081.1:g.213546C=
NG_013081.2:g.213546C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.11456-3C= MANE Select	ENSP00000265104.4:n.11456-3C=
ENST00000681290.1:c.11411-3C=	ENSP00000505288.1:n.11411-3C=
ENST00000265104.4:c.11456-3C=	ENSP00000265104.4:n.11456-3C=
NM_001369.2:c.11456-3C=	NP_001360.1:n.11456-3C=
XM_005248262.2:c.11411-3C=	XP_005248319.1:n.11411-3C=
XM_005248262.3:c.11564-3C=	XP_005248319.2:n.11564-3C=
XM_017009177.1:c.11564-3C=	XP_016864666.1:n.11564-3C=
XM_017009178.1:c.10469-3C=	XP_016864667.1:n.10469-3C=
XM_017009179.2:c.10469-3C=	XP_016864668.1:n.10469-3C=
XM_017009180.1:c.11564-3C=	XP_016864669.1:n.11564-3C=
XM_017009181.1:c.11564-3C=	XP_016864670.1:n.11564-3C=
XM_017009182.1:c.11320-3C=	XP_016864671.1:n.11320-3C=
XM_017009185.1:c.6653-3C=	XP_016864674.1:n.6653-3C=
XM_017009186.1:c.6206-3C=	XP_016864675.1:n.6206-3C=
XM_017009188.1:c.5543-3C=	XP_016864677.1:n.5543-3C=
XM_024454388.1:c.10469-3C=	XP_024310156.1:n.10469-3C=
XM_024454389.1:c.10058-3C=	XP_024310157.1:n.10058-3C=
NM_001369.3:c.11456-3C= MANE Select	NP_001360.1:n.11456-3C=