Canonical Allele Identifier: CA359224499
Community Standard Title: NM_001369.3(DNAH5):c.4348C>A (p.Gln1450Lys)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13865675G>T , CM000667.2:g.13865675G>T GRCh38
NC_000005.9:g.13865784G>T , CM000667.1:g.13865784G>T GRCh37
NC_000005.8:g.13918784G>T NCBI36
NG_013081.1:g.83806C>A
NG_013081.2:g.83806C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.4348C>A MANE Select NP_001360.1:p.Gln1450Lys
ENST00000265104.5:c.4348C>A MANE Select ENSP00000265104.4:p.Gln1450Lys
NM_001369.2:c.4348C>A NP_001360.1:p.Gln1450Lys
ENST00000265104.4:c.4348C>A ENSP00000265104.4:p.Gln1450Lys
ENST00000681290.1:c.4303C>A ENSP00000505288.1:p.Gln1435Lys
XM_005248262.2:c.4303C>A XP_005248319.1:p.Gln1435Lys
XM_005248262.3:c.4456C>A XP_005248319.2:p.Gln1486Lys
XM_011513990.1:c.4348C>A XP_011512292.1:p.Gln1450Lys
XM_017009177.1:c.4456C>A XP_016864666.1:p.Gln1486Lys
XM_017009178.1:c.3361C>A XP_016864667.1:p.Gln1121Lys
XM_017009179.2:c.3361C>A XP_016864668.1:p.Gln1121Lys
XM_017009180.1:c.4456C>A XP_016864669.1:p.Gln1486Lys
XM_017009181.1:c.4456C>A XP_016864670.1:p.Gln1486Lys
XM_017009182.1:c.4456C>A XP_016864671.1:p.Gln1486Lys
XM_017009183.1:c.4456C>A XP_016864672.1:p.Gln1486Lys
XM_017009184.1:c.4456C>A XP_016864673.1:p.Gln1486Lys
XM_017009187.1:c.4456C>A XP_016864676.1:p.Gln1486Lys
XM_024454388.1:c.3361C>A XP_024310156.1:p.Gln1121Lys
XM_024454389.1:c.2950C>A XP_024310157.1:p.Gln984Lys
XR_001742034.1:n.4473C>A
XR_001742035.1:n.4473C>A
XR_925598.1:n.4555C>A