Canonical Allele Identifier: CA1528423495

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753391T= , CM000667.2:g.13753391T=	GRCh38
NC_000005.9:g.13753500T= , CM000667.1:g.13753500T=	GRCh37
NC_000005.8:g.13806500T=	NCBI36
NG_013081.1:g.196090A=
NG_013081.2:g.196090A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10714A= MANE Select	ENSP00000265104.4:p.Thr3572=
ENST00000681290.1:c.10669A=	ENSP00000505288.1:p.Thr3557=
ENST00000265104.4:c.10714A=	ENSP00000265104.4:p.Thr3572=
NM_001369.2:c.10714A=	NP_001360.1:p.Thr3572=
XM_005248262.2:c.10669A=	XP_005248319.1:p.Thr3557=
XM_005248262.3:c.10822A=	XP_005248319.2:p.Thr3608=
XM_017009177.1:c.10822A=	XP_016864666.1:p.Thr3608=
XM_017009178.1:c.9727A=	XP_016864667.1:p.Thr3243=
XM_017009179.2:c.9727A=	XP_016864668.1:p.Thr3243=
XM_017009180.1:c.10822A=	XP_016864669.1:p.Thr3608=
XM_017009181.1:c.10822A=	XP_016864670.1:p.Thr3608=
XM_017009182.1:c.10822A=	XP_016864671.1:p.Thr3608=
XM_017009185.1:c.5911A=	XP_016864674.1:p.Thr1971=
XM_017009186.1:c.5464A=	XP_016864675.1:p.Thr1822=
XM_017009188.1:c.4801A=	XP_016864677.1:p.Thr1601=
XM_024454388.1:c.9727A=	XP_024310156.1:p.Thr3243=
XM_024454389.1:c.9316A=	XP_024310157.1:p.Thr3106=
NM_001369.3:c.10714A= MANE Select	NP_001360.1:p.Thr3572=