Canonical Allele Identifier: CA1528395876

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692090G= , CM000667.2:g.13692090G=	GRCh38
NC_000005.9:g.13692199G= , CM000667.1:g.13692199G=	GRCh37
NC_000005.8:g.13745199G=	NCBI36
NG_013081.1:g.257391C=
NG_013081.2:g.257391C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1102C=
ENST00000265104.5:c.13769C= MANE Select	ENSP00000265104.4:p.Pro4590=
ENST00000681290.1:c.13724C=	ENSP00000505288.1:p.Pro4575=
ENST00000265104.4:c.13769C=	ENSP00000265104.4:p.Pro4590=
NM_001369.2:c.13769C=	NP_001360.1:p.Pro4590=
XM_005248262.2:c.13724C=	XP_005248319.1:p.Pro4575=
XM_005248262.3:c.13877C=	XP_005248319.2:p.Pro4626=
XM_017009177.1:c.13457C=	XP_016864666.1:p.Pro4486=
XM_017009178.1:c.12782C=	XP_016864667.1:p.Pro4261=
XM_017009179.2:c.12782C=	XP_016864668.1:p.Pro4261=
XM_017009185.1:c.8966C=	XP_016864674.1:p.Pro2989=
XM_017009186.1:c.8519C=	XP_016864675.1:p.Pro2840=
XM_017009188.1:c.7856C=	XP_016864677.1:p.Pro2619=
XM_024454388.1:c.12782C=	XP_024310156.1:p.Pro4261=
XM_024454389.1:c.12371C=	XP_024310157.1:p.Pro4124=
NM_001369.3:c.13769C= MANE Select	NP_001360.1:p.Pro4590=