Canonical Allele Identifier: CA3204264
Community Standard Title: NM_001369.3(DNAH5):c.3446A>G (p.Gln1149Arg)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13871716T>C , CM000667.2:g.13871716T>C GRCh38
NC_000005.9:g.13871825T>C , CM000667.1:g.13871825T>C GRCh37
NC_000005.8:g.13924825T>C NCBI36
NG_013081.1:g.77765A>G
NG_013081.2:g.77765A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.3446A>G MANE Select NP_001360.1:p.Gln1149Arg
ENST00000265104.5:c.3446A>G MANE Select ENSP00000265104.4:p.Gln1149Arg
NM_001369.2:c.3446A>G NP_001360.1:p.Gln1149Arg
ENST00000265104.4:c.3446A>G ENSP00000265104.4:p.Gln1149Arg
ENST00000681290.1:c.3401A>G ENSP00000505288.1:p.Gln1134Arg
XM_005248262.2:c.3401A>G XP_005248319.1:p.Gln1134Arg
XM_005248262.3:c.3554A>G XP_005248319.2:p.Gln1185Arg
XM_011513990.1:c.3446A>G XP_011512292.1:p.Gln1149Arg
XM_017009177.1:c.3554A>G XP_016864666.1:p.Gln1185Arg
XM_017009178.1:c.2459A>G XP_016864667.1:p.Gln820Arg
XM_017009179.2:c.2459A>G XP_016864668.1:p.Gln820Arg
XM_017009180.1:c.3554A>G XP_016864669.1:p.Gln1185Arg
XM_017009181.1:c.3554A>G XP_016864670.1:p.Gln1185Arg
XM_017009182.1:c.3554A>G XP_016864671.1:p.Gln1185Arg
XM_017009183.1:c.3554A>G XP_016864672.1:p.Gln1185Arg
XM_017009184.1:c.3554A>G XP_016864673.1:p.Gln1185Arg
XM_017009187.1:c.3554A>G XP_016864676.1:p.Gln1185Arg
XM_024454388.1:c.2459A>G XP_024310156.1:p.Gln820Arg
XM_024454389.1:c.2048A>G XP_024310157.1:p.Gln683Arg
XR_001742034.1:n.3571A>G
XR_001742035.1:n.3571A>G
XR_925598.1:n.3653A>G