Canonical Allele Identifier: CA1528414832

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735205G= , CM000667.2:g.13735205G=	GRCh38
NC_000005.9:g.13735314G= , CM000667.1:g.13735314G=	GRCh37
NC_000005.8:g.13788314G=	NCBI36
NG_013081.1:g.214276C=
NG_013081.2:g.214276C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.11687C= MANE Select	ENSP00000265104.4:p.Thr3896=
ENST00000681290.1:c.11642C=	ENSP00000505288.1:p.Thr3881=
ENST00000265104.4:c.11687C=	ENSP00000265104.4:p.Thr3896=
NM_001369.2:c.11687C=	NP_001360.1:p.Thr3896=
XM_005248262.2:c.11642C=	XP_005248319.1:p.Thr3881=
XM_005248262.3:c.11795C=	XP_005248319.2:p.Thr3932=
XM_017009177.1:c.11795C=	XP_016864666.1:p.Thr3932=
XM_017009178.1:c.10700C=	XP_016864667.1:p.Thr3567=
XM_017009179.2:c.10700C=	XP_016864668.1:p.Thr3567=
XM_017009180.1:c.11795C=	XP_016864669.1:p.Thr3932=
XM_017009181.1:c.11795C=	XP_016864670.1:p.Thr3932=
XM_017009185.1:c.6884C=	XP_016864674.1:p.Thr2295=
XM_017009186.1:c.6437C=	XP_016864675.1:p.Thr2146=
XM_017009188.1:c.5774C=	XP_016864677.1:p.Thr1925=
XM_024454388.1:c.10700C=	XP_024310156.1:p.Thr3567=
XM_024454389.1:c.10289C=	XP_024310157.1:p.Thr3430=
NM_001369.3:c.11687C= MANE Select	NP_001360.1:p.Thr3896=