Canonical Allele Identifier: CA113925311
Community Standard Title: NM_001369.3(DNAH5):c.7096C>T (p.Arg2366Trp)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13814739G>A , CM000667.2:g.13814739G>A GRCh38
NC_000005.9:g.13814848G>A , CM000667.1:g.13814848G>A GRCh37
NC_000005.8:g.13867848G>A NCBI36
NG_013081.1:g.134742C>T
NG_013081.2:g.134742C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.7096C>T MANE Select NP_001360.1:p.Arg2366Trp
ENST00000265104.5:c.7096C>T MANE Select ENSP00000265104.4:p.Arg2366Trp
NM_001369.2:c.7096C>T NP_001360.1:p.Arg2366Trp
ENST00000265104.4:c.7096C>T ENSP00000265104.4:p.Arg2366Trp
ENST00000681290.1:c.7051C>T ENSP00000505288.1:p.Arg2351Trp
XM_005248262.2:c.7051C>T XP_005248319.1:p.Arg2351Trp
XM_005248262.3:c.7204C>T XP_005248319.2:p.Arg2402Trp
XM_011513990.1:c.7096C>T XP_011512292.1:p.Arg2366Trp
XM_017009177.1:c.7204C>T XP_016864666.1:p.Arg2402Trp
XM_017009178.1:c.6109C>T XP_016864667.1:p.Arg2037Trp
XM_017009179.2:c.6109C>T XP_016864668.1:p.Arg2037Trp
XM_017009180.1:c.7204C>T XP_016864669.1:p.Arg2402Trp
XM_017009181.1:c.7204C>T XP_016864670.1:p.Arg2402Trp
XM_017009182.1:c.7204C>T XP_016864671.1:p.Arg2402Trp
XM_017009183.1:c.7204C>T XP_016864672.1:p.Arg2402Trp
XM_017009184.1:c.7204C>T XP_016864673.1:p.Arg2402Trp
XM_017009185.1:c.2293C>T XP_016864674.1:p.Arg765Trp
XM_017009186.1:c.1846C>T XP_016864675.1:p.Arg616Trp
XM_017009187.1:c.7204C>T XP_016864676.1:p.Arg2402Trp
XM_017009188.1:c.1183C>T XP_016864677.1:p.Arg395Trp
XM_024454388.1:c.6109C>T XP_024310156.1:p.Arg2037Trp
XM_024454389.1:c.5698C>T XP_024310157.1:p.Arg1900Trp
XR_001742034.1:n.7221C>T
XR_001742035.1:n.7221C>T
XR_925598.1:n.7303C>T