Canonical Allele Identifier: CA1528423543

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753512A= , CM000667.2:g.13753512A=	GRCh38
NC_000005.9:g.13753621A= , CM000667.1:g.13753621A=	GRCh37
NC_000005.8:g.13806621A=	NCBI36
NG_013081.1:g.195969T=
NG_013081.2:g.195969T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10593T= MANE Select	ENSP00000265104.4:p.Ser3531=
ENST00000681290.1:c.10548T=	ENSP00000505288.1:p.Ser3516=
ENST00000265104.4:c.10593T=	ENSP00000265104.4:p.Ser3531=
NM_001369.2:c.10593T=	NP_001360.1:p.Ser3531=
XM_005248262.2:c.10548T=	XP_005248319.1:p.Ser3516=
XM_005248262.3:c.10701T=	XP_005248319.2:p.Ser3567=
XM_017009177.1:c.10701T=	XP_016864666.1:p.Ser3567=
XM_017009178.1:c.9606T=	XP_016864667.1:p.Ser3202=
XM_017009179.2:c.9606T=	XP_016864668.1:p.Ser3202=
XM_017009180.1:c.10701T=	XP_016864669.1:p.Ser3567=
XM_017009181.1:c.10701T=	XP_016864670.1:p.Ser3567=
XM_017009182.1:c.10701T=	XP_016864671.1:p.Ser3567=
XM_017009185.1:c.5790T=	XP_016864674.1:p.Ser1930=
XM_017009186.1:c.5343T=	XP_016864675.1:p.Ser1781=
XM_017009188.1:c.4680T=	XP_016864677.1:p.Ser1560=
XM_024454388.1:c.9606T=	XP_024310156.1:p.Ser3202=
XM_024454389.1:c.9195T=	XP_024310157.1:p.Ser3065=
NM_001369.3:c.10593T= MANE Select	NP_001360.1:p.Ser3531=