Canonical Allele Identifier: CA1528431229

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770895C= , CM000667.2:g.13770895C=	GRCh38
NC_000005.9:g.13771004C= , CM000667.1:g.13771004C=	GRCh37
NC_000005.8:g.13824004C=	NCBI36
NG_013081.1:g.178586G=
NG_013081.2:g.178586G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9459G= MANE Select	ENSP00000265104.4:p.Gln3153=
ENST00000681290.1:c.9414G=	ENSP00000505288.1:p.Gln3138=
ENST00000265104.4:c.9459G=	ENSP00000265104.4:p.Gln3153=
ENST00000504001.3:n.171G=
NM_001369.2:c.9459G=	NP_001360.1:p.Gln3153=
XM_005248262.2:c.9414G=	XP_005248319.1:p.Gln3138=
XM_005248262.3:c.9567G=	XP_005248319.2:p.Gln3189=
XM_017009177.1:c.9567G=	XP_016864666.1:p.Gln3189=
XM_017009178.1:c.8472G=	XP_016864667.1:p.Gln2824=
XM_017009179.2:c.8472G=	XP_016864668.1:p.Gln2824=
XM_017009180.1:c.9567G=	XP_016864669.1:p.Gln3189=
XM_017009181.1:c.9567G=	XP_016864670.1:p.Gln3189=
XM_017009182.1:c.9567G=	XP_016864671.1:p.Gln3189=
XM_017009183.1:c.9567G=	XP_016864672.1:p.Gln3189=
XM_017009185.1:c.4656G=	XP_016864674.1:p.Gln1552=
XM_017009186.1:c.4209G=	XP_016864675.1:p.Gln1403=
XM_017009188.1:c.3546G=	XP_016864677.1:p.Gln1182=
XM_024454388.1:c.8472G=	XP_024310156.1:p.Gln2824=
XM_024454389.1:c.8061G=	XP_024310157.1:p.Gln2687=
NM_001369.3:c.9459G= MANE Select	NP_001360.1:p.Gln3153=