Canonical Allele Identifier: CA1528427630

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13762777C= , CM000667.2:g.13762777C=	GRCh38
NC_000005.9:g.13762886C= , CM000667.1:g.13762886C=	GRCh37
NC_000005.8:g.13815886C=	NCBI36
NG_013081.1:g.186704G=
NG_013081.2:g.186704G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10226G= MANE Select	ENSP00000265104.4:p.Trp3409=
ENST00000681290.1:c.10181G=	ENSP00000505288.1:p.Trp3394=
ENST00000265104.4:c.10226G=	ENSP00000265104.4:p.Trp3409=
ENST00000504001.3:n.734G=
NM_001369.2:c.10226G=	NP_001360.1:p.Trp3409=
XM_005248262.2:c.10181G=	XP_005248319.1:p.Trp3394=
XM_005248262.3:c.10334G=	XP_005248319.2:p.Trp3445=
XM_017009177.1:c.10334G=	XP_016864666.1:p.Trp3445=
XM_017009178.1:c.9239G=	XP_016864667.1:p.Trp3080=
XM_017009179.2:c.9239G=	XP_016864668.1:p.Trp3080=
XM_017009180.1:c.10334G=	XP_016864669.1:p.Trp3445=
XM_017009181.1:c.10334G=	XP_016864670.1:p.Trp3445=
XM_017009182.1:c.10334G=	XP_016864671.1:p.Trp3445=
XM_017009185.1:c.5423G=	XP_016864674.1:p.Trp1808=
XM_017009186.1:c.4976G=	XP_016864675.1:p.Trp1659=
XM_017009188.1:c.4313G=	XP_016864677.1:p.Trp1438=
XM_024454388.1:c.9239G=	XP_024310156.1:p.Trp3080=
XM_024454389.1:c.8828G=	XP_024310157.1:p.Trp2943=
NM_001369.3:c.10226G= MANE Select	NP_001360.1:p.Trp3409=