Canonical Allele Identifier: CA3203643
Community Standard Title: NM_001369.3(DNAH5):c.5539A>G (p.Arg1847Gly)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13841076T>C , CM000667.2:g.13841076T>C GRCh38
NC_000005.9:g.13841185T>C , CM000667.1:g.13841185T>C GRCh37
NC_000005.8:g.13894185T>C NCBI36
NG_013081.1:g.108405A>G
NG_013081.2:g.108405A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.5539A>G MANE Select NP_001360.1:p.Arg1847Gly
ENST00000265104.5:c.5539A>G MANE Select ENSP00000265104.4:p.Arg1847Gly
NM_001369.2:c.5539A>G NP_001360.1:p.Arg1847Gly
ENST00000265104.4:c.5539A>G ENSP00000265104.4:p.Arg1847Gly
ENST00000681290.1:c.5494A>G ENSP00000505288.1:p.Arg1832Gly
XM_005248262.2:c.5494A>G XP_005248319.1:p.Arg1832Gly
XM_005248262.3:c.5647A>G XP_005248319.2:p.Arg1883Gly
XM_011513990.1:c.5539A>G XP_011512292.1:p.Arg1847Gly
XM_017009177.1:c.5647A>G XP_016864666.1:p.Arg1883Gly
XM_017009178.1:c.4552A>G XP_016864667.1:p.Arg1518Gly
XM_017009179.2:c.4552A>G XP_016864668.1:p.Arg1518Gly
XM_017009180.1:c.5647A>G XP_016864669.1:p.Arg1883Gly
XM_017009181.1:c.5647A>G XP_016864670.1:p.Arg1883Gly
XM_017009182.1:c.5647A>G XP_016864671.1:p.Arg1883Gly
XM_017009183.1:c.5647A>G XP_016864672.1:p.Arg1883Gly
XM_017009184.1:c.5647A>G XP_016864673.1:p.Arg1883Gly
XM_017009185.1:c.736A>G XP_016864674.1:p.Arg246Gly
XM_017009186.1:c.289A>G XP_016864675.1:p.Arg97Gly
XM_017009187.1:c.5647A>G XP_016864676.1:p.Arg1883Gly
XM_024454388.1:c.4552A>G XP_024310156.1:p.Arg1518Gly
XM_024454389.1:c.4141A>G XP_024310157.1:p.Arg1381Gly
XR_001742034.1:n.5664A>G
XR_001742035.1:n.5664A>G
XR_925598.1:n.5746A>G