Canonical Allele Identifier: CA1528435453

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776701A= , CM000667.2:g.13776701A=	GRCh38
NC_000005.9:g.13776810A= , CM000667.1:g.13776810A=	GRCh37
NC_000005.8:g.13829810A=	NCBI36
NG_013081.1:g.172780T=
NG_013081.2:g.172780T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9111T= MANE Select	ENSP00000265104.4:p.Ser3037=
ENST00000681290.1:c.9066T=	ENSP00000505288.1:p.Ser3022=
ENST00000265104.4:c.9111T=	ENSP00000265104.4:p.Ser3037=
NM_001369.2:c.9111T=	NP_001360.1:p.Ser3037=
XM_005248262.2:c.9066T=	XP_005248319.1:p.Ser3022=
XM_011513990.1:c.9106T=	XP_011512292.1:p.Ter3036=
XR_925598.1:n.9182T=
XM_005248262.3:c.9219T=	XP_005248319.2:p.Ser3073=
XM_017009177.1:c.9219T=	XP_016864666.1:p.Ser3073=
XM_017009178.1:c.8124T=	XP_016864667.1:p.Ser2708=
XM_017009179.2:c.8124T=	XP_016864668.1:p.Ser2708=
XM_017009180.1:c.9219T=	XP_016864669.1:p.Ser3073=
XM_017009181.1:c.9219T=	XP_016864670.1:p.Ser3073=
XM_017009182.1:c.9219T=	XP_016864671.1:p.Ser3073=
XM_017009183.1:c.9219T=	XP_016864672.1:p.Ser3073=
XM_017009184.1:c.9214T=	XP_016864673.1:p.Ter3072=
XM_017009185.1:c.4308T=	XP_016864674.1:p.Ser1436=
XM_017009186.1:c.3861T=	XP_016864675.1:p.Ser1287=
XM_017009188.1:c.3198T=	XP_016864677.1:p.Ser1066=
XM_024454388.1:c.8124T=	XP_024310156.1:p.Ser2708=
XM_024454389.1:c.7713T=	XP_024310157.1:p.Ser2571=
XR_001742034.1:n.9105T=
XR_001742035.1:n.9100T=
NM_001369.3:c.9111T= MANE Select	NP_001360.1:p.Ser3037=