Canonical Allele Identifier: CA443536802

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13901523G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13901414G>T , CM000667.2:g.13901414G>T	GRCh38
NC_000005.9:g.13901523G>T , CM000667.1:g.13901523G>T	GRCh37
NC_000005.8:g.13954523G>T	NCBI36
NG_013081.1:g.48067C>A
NG_013081.2:g.48067C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.1890C>A MANE Select	ENSP00000265104.4:p.Ala630=
ENST00000681290.1:c.1845C>A	ENSP00000505288.1:p.Ala615=
ENST00000265104.4:c.1890C>A	ENSP00000265104.4:p.Ala630=
NM_001369.2:c.1890C>A	NP_001360.1:p.Ala630=
XM_005248262.2:c.1845C>A	XP_005248319.1:p.Ala615=
XM_011513990.1:c.1890C>A	XP_011512292.1:p.Ala630=
XR_925598.1:n.2097C>A
XM_005248262.3:c.1998C>A	XP_005248319.2:p.Ala666=
XM_017009177.1:c.1998C>A	XP_016864666.1:p.Ala666=
XM_017009178.1:c.903C>A	XP_016864667.1:p.Ala301=
XM_017009179.2:c.903C>A	XP_016864668.1:p.Ala301=
XM_017009180.1:c.1998C>A	XP_016864669.1:p.Ala666=
XM_017009181.1:c.1998C>A	XP_016864670.1:p.Ala666=
XM_017009182.1:c.1998C>A	XP_016864671.1:p.Ala666=
XM_017009183.1:c.1998C>A	XP_016864672.1:p.Ala666=
XM_017009184.1:c.1998C>A	XP_016864673.1:p.Ala666=
XM_017009187.1:c.1998C>A	XP_016864676.1:p.Ala666=
XM_024454388.1:c.903C>A	XP_024310156.1:p.Ala301=
XM_024454389.1:c.492C>A	XP_024310157.1:p.Ala164=
XR_001742034.1:n.2015C>A
XR_001742035.1:n.2015C>A
NM_001369.3:c.1890C>A MANE Select	NP_001360.1:p.Ala630=