Canonical Allele Identifier: CA2739274635

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 2843315
• ClinVar RCV Id: RCV003652446

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13871010A>T , CM000667.2:g.13871010A>T	GRCh38
NC_000005.9:g.13871119A>T , CM000667.1:g.13871119A>T	GRCh37
NC_000005.8:g.13924119A>T	NCBI36
NG_013081.1:g.78471T>A
NG_013081.2:g.78471T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.3599-8T>A MANE Select	ENSP00000265104.4:n.3599-8T>A
ENST00000681290.1:c.3554-8T>A	ENSP00000505288.1:n.3554-8T>A
ENST00000265104.4:c.3599-8T>A	ENSP00000265104.4:n.3599-8T>A
NM_001369.2:c.3599-8T>A	NP_001360.1:n.3599-8T>A
XM_005248262.2:c.3554-8T>A	XP_005248319.1:n.3554-8T>A
XM_011513990.1:c.3599-8T>A	XP_011512292.1:n.3599-8T>A
XR_925598.1:n.3806-8T>A
XM_005248262.3:c.3707-8T>A	XP_005248319.2:n.3707-8T>A
XM_017009177.1:c.3707-8T>A	XP_016864666.1:n.3707-8T>A
XM_017009178.1:c.2612-8T>A	XP_016864667.1:n.2612-8T>A
XM_017009179.2:c.2612-8T>A	XP_016864668.1:n.2612-8T>A
XM_017009180.1:c.3707-8T>A	XP_016864669.1:n.3707-8T>A
XM_017009181.1:c.3707-8T>A	XP_016864670.1:n.3707-8T>A
XM_017009182.1:c.3707-8T>A	XP_016864671.1:n.3707-8T>A
XM_017009183.1:c.3707-8T>A	XP_016864672.1:n.3707-8T>A
XM_017009184.1:c.3707-8T>A	XP_016864673.1:n.3707-8T>A
XM_017009187.1:c.3707-8T>A	XP_016864676.1:n.3707-8T>A
XM_024454388.1:c.2612-8T>A	XP_024310156.1:n.2612-8T>A
XM_024454389.1:c.2201-8T>A	XP_024310157.1:n.2201-8T>A
XR_001742034.1:n.3724-8T>A
XR_001742035.1:n.3724-8T>A
NM_001369.3:c.3599-8T>A MANE Select	NP_001360.1:n.3599-8T>A