Canonical Allele Identifier: CA359209561
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13776664T>G , CM000667.2:g.13776664T>G GRCh38
NC_000005.9:g.13776773T>G , CM000667.1:g.13776773T>G GRCh37
NC_000005.8:g.13829773T>G NCBI36
NG_013081.1:g.172817A>C
NG_013081.2:g.172817A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9148A>C MANE Select ENSP00000265104.4:p.Ser3050Arg
ENST00000681290.1:c.9103A>C ENSP00000505288.1:p.Ser3035Arg
ENST00000265104.4:c.9148A>C ENSP00000265104.4:p.Ser3050Arg
NM_001369.2:c.9148A>C NP_001360.1:p.Ser3050Arg
XM_005248262.2:c.9103A>C XP_005248319.1:p.Ser3035Arg
XM_011513990.1:c.*35A>C XP_011512292.1:n.*35A>C
XR_925598.1:n.9219A>C
XM_005248262.3:c.9256A>C XP_005248319.2:p.Ser3086Arg
XM_017009177.1:c.9256A>C XP_016864666.1:p.Ser3086Arg
XM_017009178.1:c.8161A>C XP_016864667.1:p.Ser2721Arg
XM_017009179.2:c.8161A>C XP_016864668.1:p.Ser2721Arg
XM_017009180.1:c.9256A>C XP_016864669.1:p.Ser3086Arg
XM_017009181.1:c.9256A>C XP_016864670.1:p.Ser3086Arg
XM_017009182.1:c.9256A>C XP_016864671.1:p.Ser3086Arg
XM_017009183.1:c.9256A>C XP_016864672.1:p.Ser3086Arg
XM_017009184.1:c.*35A>C XP_016864673.1:n.*35A>C
XM_017009185.1:c.4345A>C XP_016864674.1:p.Ser1449Arg
XM_017009186.1:c.3898A>C XP_016864675.1:p.Ser1300Arg
XM_017009188.1:c.3235A>C XP_016864677.1:p.Ser1079Arg
XM_024454388.1:c.8161A>C XP_024310156.1:p.Ser2721Arg
XM_024454389.1:c.7750A>C XP_024310157.1:p.Ser2584Arg
XR_001742034.1:n.9142A>C
XR_001742035.1:n.9137A>C
NM_001369.3:c.9148A>C MANE Select NP_001360.1:p.Ser3050Arg