Canonical Allele Identifier: CA1528435295

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776616T= , CM000667.2:g.13776616T=	GRCh38
NC_000005.9:g.13776725T= , CM000667.1:g.13776725T=	GRCh37
NC_000005.8:g.13829725T=	NCBI36
NG_013081.1:g.172865A=
NG_013081.2:g.172865A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9196A= MANE Select	ENSP00000265104.4:p.Thr3066=
ENST00000681290.1:c.9151A=	ENSP00000505288.1:p.Thr3051=
ENST00000265104.4:c.9196A=	ENSP00000265104.4:p.Thr3066=
NM_001369.2:c.9196A=	NP_001360.1:p.Thr3066=
XM_005248262.2:c.9151A=	XP_005248319.1:p.Thr3051=
XM_005248262.3:c.9304A=	XP_005248319.2:p.Thr3102=
XM_017009177.1:c.9304A=	XP_016864666.1:p.Thr3102=
XM_017009178.1:c.8209A=	XP_016864667.1:p.Thr2737=
XM_017009179.2:c.8209A=	XP_016864668.1:p.Thr2737=
XM_017009180.1:c.9304A=	XP_016864669.1:p.Thr3102=
XM_017009181.1:c.9304A=	XP_016864670.1:p.Thr3102=
XM_017009182.1:c.9304A=	XP_016864671.1:p.Thr3102=
XM_017009183.1:c.9304A=	XP_016864672.1:p.Thr3102=
XM_017009185.1:c.4393A=	XP_016864674.1:p.Thr1465=
XM_017009186.1:c.3946A=	XP_016864675.1:p.Thr1316=
XM_017009188.1:c.3283A=	XP_016864677.1:p.Thr1095=
XM_024454388.1:c.8209A=	XP_024310156.1:p.Thr2737=
XM_024454389.1:c.7798A=	XP_024310157.1:p.Thr2600=
NM_001369.3:c.9196A= MANE Select	NP_001360.1:p.Thr3066=