Canonical Allele Identifier: CA113982205

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13871719C>T , CM000667.2:g.13871719C>T	GRCh38
NC_000005.9:g.13871828C>T , CM000667.1:g.13871828C>T	GRCh37
NC_000005.8:g.13924828C>T	NCBI36
NG_013081.1:g.77762G>A
NG_013081.2:g.77762G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.3443G>A MANE Select	NP_001360.1:p.Trp1148Ter
ENST00000265104.5:c.3443G>A MANE Select	ENSP00000265104.4:p.Trp1148Ter
NM_001369.2:c.3443G>A	NP_001360.1:p.Trp1148Ter
ENST00000265104.4:c.3443G>A	ENSP00000265104.4:p.Trp1148Ter
ENST00000681290.1:c.3398G>A	ENSP00000505288.1:p.Trp1133Ter
XM_005248262.2:c.3398G>A	XP_005248319.1:p.Trp1133Ter
XM_005248262.3:c.3551G>A	XP_005248319.2:p.Trp1184Ter
XM_011513990.1:c.3443G>A	XP_011512292.1:p.Trp1148Ter
XM_017009177.1:c.3551G>A	XP_016864666.1:p.Trp1184Ter
XM_017009178.1:c.2456G>A	XP_016864667.1:p.Trp819Ter
XM_017009179.2:c.2456G>A	XP_016864668.1:p.Trp819Ter
XM_017009180.1:c.3551G>A	XP_016864669.1:p.Trp1184Ter
XM_017009181.1:c.3551G>A	XP_016864670.1:p.Trp1184Ter
XM_017009182.1:c.3551G>A	XP_016864671.1:p.Trp1184Ter
XM_017009183.1:c.3551G>A	XP_016864672.1:p.Trp1184Ter
XM_017009184.1:c.3551G>A	XP_016864673.1:p.Trp1184Ter
XM_017009187.1:c.3551G>A	XP_016864676.1:p.Trp1184Ter
XM_024454388.1:c.2456G>A	XP_024310156.1:p.Trp819Ter
XM_024454389.1:c.2045G>A	XP_024310157.1:p.Trp682Ter
XR_001742034.1:n.3568G>A
XR_001742035.1:n.3568G>A
XR_925598.1:n.3650G>A