Canonical Allele Identifier: CA359216914

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13850707G>A , CM000667.2:g.13850707G>A	GRCh38
NC_000005.9:g.13850816G>A , CM000667.1:g.13850816G>A	GRCh37
NC_000005.8:g.13903816G>A	NCBI36
NG_013081.1:g.98774C>T
NG_013081.2:g.98774C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.5059C>T MANE Select	NP_001360.1:p.Gln1687Ter
ENST00000265104.5:c.5059C>T MANE Select	ENSP00000265104.4:p.Gln1687Ter
NM_001369.2:c.5059C>T	NP_001360.1:p.Gln1687Ter
ENST00000265104.4:c.5059C>T	ENSP00000265104.4:p.Gln1687Ter
ENST00000681290.1:c.5014C>T	ENSP00000505288.1:p.Gln1672Ter
XM_005248262.2:c.5014C>T	XP_005248319.1:p.Gln1672Ter
XM_005248262.3:c.5167C>T	XP_005248319.2:p.Gln1723Ter
XM_011513990.1:c.5059C>T	XP_011512292.1:p.Gln1687Ter
XM_017009177.1:c.5167C>T	XP_016864666.1:p.Gln1723Ter
XM_017009178.1:c.4072C>T	XP_016864667.1:p.Gln1358Ter
XM_017009179.2:c.4072C>T	XP_016864668.1:p.Gln1358Ter
XM_017009180.1:c.5167C>T	XP_016864669.1:p.Gln1723Ter
XM_017009181.1:c.5167C>T	XP_016864670.1:p.Gln1723Ter
XM_017009182.1:c.5167C>T	XP_016864671.1:p.Gln1723Ter
XM_017009183.1:c.5167C>T	XP_016864672.1:p.Gln1723Ter
XM_017009184.1:c.5167C>T	XP_016864673.1:p.Gln1723Ter
XM_017009185.1:c.256C>T	XP_016864674.1:p.Gln86Ter
XM_017009186.1:c.-35C>T	XP_016864675.1:n.-35C>T
XM_017009187.1:c.5167C>T	XP_016864676.1:p.Gln1723Ter
XM_024454388.1:c.4072C>T	XP_024310156.1:p.Gln1358Ter
XM_024454389.1:c.3661C>T	XP_024310157.1:p.Gln1221Ter
XR_001742034.1:n.5184C>T
XR_001742035.1:n.5184C>T
XR_925598.1:n.5266C>T