Canonical Allele Identifier: CA113954672
Community Standard Title: NM_001369.3(DNAH5):c.5147G>T (p.Arg1716Leu)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13844961C>A , CM000667.2:g.13844961C>A GRCh38
NC_000005.9:g.13845070C>A , CM000667.1:g.13845070C>A GRCh37
NC_000005.8:g.13898070C>A NCBI36
NG_013081.1:g.104520G>T
NG_013081.2:g.104520G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.5147G>T MANE Select NP_001360.1:p.Arg1716Leu
ENST00000265104.5:c.5147G>T MANE Select ENSP00000265104.4:p.Arg1716Leu
NM_001369.2:c.5147G>T NP_001360.1:p.Arg1716Leu
ENST00000265104.4:c.5147G>T ENSP00000265104.4:p.Arg1716Leu
ENST00000681290.1:c.5102G>T ENSP00000505288.1:p.Arg1701Leu
XM_005248262.2:c.5102G>T XP_005248319.1:p.Arg1701Leu
XM_005248262.3:c.5255G>T XP_005248319.2:p.Arg1752Leu
XM_011513990.1:c.5147G>T XP_011512292.1:p.Arg1716Leu
XM_017009177.1:c.5255G>T XP_016864666.1:p.Arg1752Leu
XM_017009178.1:c.4160G>T XP_016864667.1:p.Arg1387Leu
XM_017009179.2:c.4160G>T XP_016864668.1:p.Arg1387Leu
XM_017009180.1:c.5255G>T XP_016864669.1:p.Arg1752Leu
XM_017009181.1:c.5255G>T XP_016864670.1:p.Arg1752Leu
XM_017009182.1:c.5255G>T XP_016864671.1:p.Arg1752Leu
XM_017009183.1:c.5255G>T XP_016864672.1:p.Arg1752Leu
XM_017009184.1:c.5255G>T XP_016864673.1:p.Arg1752Leu
XM_017009185.1:c.344G>T XP_016864674.1:p.Arg115Leu
XM_017009186.1:c.22-3057G>T XP_016864675.1:n.22-3057G>T
XM_017009187.1:c.5255G>T XP_016864676.1:p.Arg1752Leu
XM_024454388.1:c.4160G>T XP_024310156.1:p.Arg1387Leu
XM_024454389.1:c.3749G>T XP_024310157.1:p.Arg1250Leu
XR_001742034.1:n.5272G>T
XR_001742035.1:n.5272G>T
XR_925598.1:n.5354G>T