Canonical Allele Identifier: CA359197067
Community Standard Title: NM_001369.3(DNAH5):c.6574A>T (p.Lys2192Ter)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13824204T>A , CM000667.2:g.13824204T>A GRCh38
NC_000005.9:g.13824313T>A , CM000667.1:g.13824313T>A GRCh37
NC_000005.8:g.13877313T>A NCBI36
NG_013081.1:g.125277A>T
NG_013081.2:g.125277A>T

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.6574A>T MANE Select NP_001360.1:p.Lys2192Ter
ENST00000265104.5:c.6574A>T MANE Select ENSP00000265104.4:p.Lys2192Ter
NM_001369.2:c.6574A>T NP_001360.1:p.Lys2192Ter
ENST00000265104.4:c.6574A>T ENSP00000265104.4:p.Lys2192Ter
ENST00000681290.1:c.6529A>T ENSP00000505288.1:p.Lys2177Ter
ENST00000683090.1:n.1505A>T
XM_005248262.2:c.6529A>T XP_005248319.1:p.Lys2177Ter
XM_005248262.3:c.6682A>T XP_005248319.2:p.Lys2228Ter
XM_011513990.1:c.6574A>T XP_011512292.1:p.Lys2192Ter
XM_017009177.1:c.6682A>T XP_016864666.1:p.Lys2228Ter
XM_017009178.1:c.5587A>T XP_016864667.1:p.Lys1863Ter
XM_017009179.2:c.5587A>T XP_016864668.1:p.Lys1863Ter
XM_017009180.1:c.6682A>T XP_016864669.1:p.Lys2228Ter
XM_017009181.1:c.6682A>T XP_016864670.1:p.Lys2228Ter
XM_017009182.1:c.6682A>T XP_016864671.1:p.Lys2228Ter
XM_017009183.1:c.6682A>T XP_016864672.1:p.Lys2228Ter
XM_017009184.1:c.6682A>T XP_016864673.1:p.Lys2228Ter
XM_017009185.1:c.1771A>T XP_016864674.1:p.Lys591Ter
XM_017009186.1:c.1324A>T XP_016864675.1:p.Lys442Ter
XM_017009187.1:c.6682A>T XP_016864676.1:p.Lys2228Ter
XM_017009188.1:c.661A>T XP_016864677.1:p.Lys221Ter
XM_024454388.1:c.5587A>T XP_024310156.1:p.Lys1863Ter
XM_024454389.1:c.5176A>T XP_024310157.1:p.Lys1726Ter
XR_001742034.1:n.6699A>T
XR_001742035.1:n.6699A>T
XR_925598.1:n.6781A>T