Canonical Allele Identifier: CA1528395842

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692010C= , CM000667.2:g.13692010C=	GRCh38
NC_000005.9:g.13692119C= , CM000667.1:g.13692119C=	GRCh37
NC_000005.8:g.13745119C=	NCBI36
NG_013081.1:g.257471G=
NG_013081.2:g.257471G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1182G=
ENST00000265104.5:c.13849G= MANE Select	ENSP00000265104.4:p.Val4617=
ENST00000681290.1:c.13804G=	ENSP00000505288.1:p.Val4602=
ENST00000265104.4:c.13849G=	ENSP00000265104.4:p.Val4617=
NM_001369.2:c.13849G=	NP_001360.1:p.Val4617=
XM_005248262.2:c.13804G=	XP_005248319.1:p.Val4602=
XM_005248262.3:c.13957G=	XP_005248319.2:p.Val4653=
XM_017009177.1:c.13537G=	XP_016864666.1:p.Val4513=
XM_017009178.1:c.12862G=	XP_016864667.1:p.Val4288=
XM_017009179.2:c.12862G=	XP_016864668.1:p.Val4288=
XM_017009185.1:c.9046G=	XP_016864674.1:p.Val3016=
XM_017009186.1:c.8599G=	XP_016864675.1:p.Val2867=
XM_017009188.1:c.7936G=	XP_016864677.1:p.Val2646=
XM_024454388.1:c.12862G=	XP_024310156.1:p.Val4288=
XM_024454389.1:c.12451G=	XP_024310157.1:p.Val4151=
NM_001369.3:c.13849G= MANE Select	NP_001360.1:p.Val4617=