Canonical Allele Identifier: CA1528435042

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776463A= , CM000667.2:g.13776463A=	GRCh38
NC_000005.9:g.13776572A= , CM000667.1:g.13776572A=	GRCh37
NC_000005.8:g.13829572A=	NCBI36
NG_013081.1:g.173018T=
NG_013081.2:g.173018T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.9349T= MANE Select	ENSP00000265104.4:p.Trp3117=
ENST00000681290.1:c.9304T=	ENSP00000505288.1:p.Trp3102=
ENST00000265104.4:c.9349T=	ENSP00000265104.4:p.Trp3117=
NM_001369.2:c.9349T=	NP_001360.1:p.Trp3117=
XM_005248262.2:c.9304T=	XP_005248319.1:p.Trp3102=
XM_005248262.3:c.9457T=	XP_005248319.2:p.Trp3153=
XM_017009177.1:c.9457T=	XP_016864666.1:p.Trp3153=
XM_017009178.1:c.8362T=	XP_016864667.1:p.Trp2788=
XM_017009179.2:c.8362T=	XP_016864668.1:p.Trp2788=
XM_017009180.1:c.9457T=	XP_016864669.1:p.Trp3153=
XM_017009181.1:c.9457T=	XP_016864670.1:p.Trp3153=
XM_017009182.1:c.9457T=	XP_016864671.1:p.Trp3153=
XM_017009183.1:c.9457T=	XP_016864672.1:p.Trp3153=
XM_017009185.1:c.4546T=	XP_016864674.1:p.Trp1516=
XM_017009186.1:c.4099T=	XP_016864675.1:p.Trp1367=
XM_017009188.1:c.3436T=	XP_016864677.1:p.Trp1146=
XM_024454388.1:c.8362T=	XP_024310156.1:p.Trp2788=
XM_024454389.1:c.7951T=	XP_024310157.1:p.Trp2651=
NM_001369.3:c.9349T= MANE Select	NP_001360.1:p.Trp3117=