Canonical Allele Identifier: CA1528423455

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753290A= , CM000667.2:g.13753290A=	GRCh38
NC_000005.9:g.13753399A= , CM000667.1:g.13753399A=	GRCh37
NC_000005.8:g.13806399A=	NCBI36
NG_013081.1:g.196191T=
NG_013081.2:g.196191T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10815T= MANE Select	ENSP00000265104.4:p.Asp3605=
ENST00000681290.1:c.10770T=	ENSP00000505288.1:p.Asp3590=
ENST00000265104.4:c.10815T=	ENSP00000265104.4:p.Asp3605=
NM_001369.2:c.10815T=	NP_001360.1:p.Asp3605=
XM_005248262.2:c.10770T=	XP_005248319.1:p.Asp3590=
XM_005248262.3:c.10923T=	XP_005248319.2:p.Asp3641=
XM_017009177.1:c.10923T=	XP_016864666.1:p.Asp3641=
XM_017009178.1:c.9828T=	XP_016864667.1:p.Asp3276=
XM_017009179.2:c.9828T=	XP_016864668.1:p.Asp3276=
XM_017009180.1:c.10923T=	XP_016864669.1:p.Asp3641=
XM_017009181.1:c.10923T=	XP_016864670.1:p.Asp3641=
XM_017009182.1:c.10923T=	XP_016864671.1:p.Asp3641=
XM_017009185.1:c.6012T=	XP_016864674.1:p.Asp2004=
XM_017009186.1:c.5565T=	XP_016864675.1:p.Asp1855=
XM_017009188.1:c.4902T=	XP_016864677.1:p.Asp1634=
XM_024454388.1:c.9828T=	XP_024310156.1:p.Asp3276=
XM_024454389.1:c.9417T=	XP_024310157.1:p.Asp3139=
NM_001369.3:c.10815T= MANE Select	NP_001360.1:p.Asp3605=