Canonical Allele Identifier: CA1528454108

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13820500C= , CM000667.2:g.13820500C=	GRCh38
NC_000005.9:g.13820609C= , CM000667.1:g.13820609C=	GRCh37
NC_000005.8:g.13873609C=	NCBI36
NG_013081.1:g.128981G=
NG_013081.2:g.128981G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.6688-1G= MANE Select	NP_001360.1:n.6688-1G=
ENST00000265104.5:c.6688-1G= MANE Select	ENSP00000265104.4:n.6688-1G=
NM_001369.2:c.6688-1G=	NP_001360.1:n.6688-1G=
ENST00000265104.4:c.6688-1G=	ENSP00000265104.4:n.6688-1G=
ENST00000681290.1:c.6643-1G=	ENSP00000505288.1:n.6643-1G=
ENST00000683090.1:n.1619-1G=
XM_005248262.2:c.6643-1G=	XP_005248319.1:n.6643-1G=
XM_005248262.3:c.6796-1G=	XP_005248319.2:n.6796-1G=
XM_011513990.1:c.6688-1G=	XP_011512292.1:n.6688-1G=
XM_017009177.1:c.6796-1G=	XP_016864666.1:n.6796-1G=
XM_017009178.1:c.5701-1G=	XP_016864667.1:n.5701-1G=
XM_017009179.2:c.5701-1G=	XP_016864668.1:n.5701-1G=
XM_017009180.1:c.6796-1G=	XP_016864669.1:n.6796-1G=
XM_017009181.1:c.6796-1G=	XP_016864670.1:n.6796-1G=
XM_017009182.1:c.6796-1G=	XP_016864671.1:n.6796-1G=
XM_017009183.1:c.6796-1G=	XP_016864672.1:n.6796-1G=
XM_017009184.1:c.6796-1G=	XP_016864673.1:n.6796-1G=
XM_017009185.1:c.1885-1G=	XP_016864674.1:n.1885-1G=
XM_017009186.1:c.1438-1G=	XP_016864675.1:n.1438-1G=
XM_017009187.1:c.6796-1G=	XP_016864676.1:n.6796-1G=
XM_017009188.1:c.775-1G=	XP_016864677.1:n.775-1G=
XM_024454388.1:c.5701-1G=	XP_024310156.1:n.5701-1G=
XM_024454389.1:c.5290-1G=	XP_024310157.1:n.5290-1G=
XR_001742034.1:n.6813-1G=
XR_001742035.1:n.6813-1G=
XR_925598.1:n.6895-1G=