Canonical Allele Identifier: CA1528430385

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13769096T= , CM000667.2:g.13769096T=	GRCh38
NC_000005.9:g.13769205T= , CM000667.1:g.13769205T=	GRCh37
NC_000005.8:g.13822205T=	NCBI36
NG_013081.1:g.180385A=
NG_013081.2:g.180385A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9761A= MANE Select	ENSP00000265104.4:p.Lys3254=
ENST00000681290.1:c.9716A=	ENSP00000505288.1:p.Lys3239=
ENST00000265104.4:c.9761A=	ENSP00000265104.4:p.Lys3254=
ENST00000504001.3:n.473A=
NM_001369.2:c.9761A=	NP_001360.1:p.Lys3254=
XM_005248262.2:c.9716A=	XP_005248319.1:p.Lys3239=
XM_005248262.3:c.9869A=	XP_005248319.2:p.Lys3290=
XM_017009177.1:c.9869A=	XP_016864666.1:p.Lys3290=
XM_017009178.1:c.8774A=	XP_016864667.1:p.Lys2925=
XM_017009179.2:c.8774A=	XP_016864668.1:p.Lys2925=
XM_017009180.1:c.9869A=	XP_016864669.1:p.Lys3290=
XM_017009181.1:c.9869A=	XP_016864670.1:p.Lys3290=
XM_017009182.1:c.9869A=	XP_016864671.1:p.Lys3290=
XM_017009185.1:c.4958A=	XP_016864674.1:p.Lys1653=
XM_017009186.1:c.4511A=	XP_016864675.1:p.Lys1504=
XM_017009188.1:c.3848A=	XP_016864677.1:p.Lys1283=
XM_024454388.1:c.8774A=	XP_024310156.1:p.Lys2925=
XM_024454389.1:c.8363A=	XP_024310157.1:p.Lys2788=
NM_001369.3:c.9761A= MANE Select	NP_001360.1:p.Lys3254=