Canonical Allele Identifier: CA1528395856
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13692044T= , CM000667.2:g.13692044T= GRCh38
NC_000005.9:g.13692153T= , CM000667.1:g.13692153T= GRCh37
NC_000005.8:g.13745153T= NCBI36
NG_013081.1:g.257437A=
NG_013081.2:g.257437A=

Transcript Alleles

HGVS Amino-acid change
ENST00000683611.1:n.1148A=
ENST00000265104.5:c.13815A= MANE Select ENSP00000265104.4:p.Thr4605=
ENST00000681290.1:c.13770A= ENSP00000505288.1:p.Thr4590=
ENST00000265104.4:c.13815A= ENSP00000265104.4:p.Thr4605=
NM_001369.2:c.13815A= NP_001360.1:p.Thr4605=
XM_005248262.2:c.13770A= XP_005248319.1:p.Thr4590=
XM_005248262.3:c.13923A= XP_005248319.2:p.Thr4641=
XM_017009177.1:c.13503A= XP_016864666.1:p.Thr4501=
XM_017009178.1:c.12828A= XP_016864667.1:p.Thr4276=
XM_017009179.2:c.12828A= XP_016864668.1:p.Thr4276=
XM_017009185.1:c.9012A= XP_016864674.1:p.Thr3004=
XM_017009186.1:c.8565A= XP_016864675.1:p.Thr2855=
XM_017009188.1:c.7902A= XP_016864677.1:p.Thr2634=
XM_024454388.1:c.12828A= XP_024310156.1:p.Thr4276=
XM_024454389.1:c.12417A= XP_024310157.1:p.Thr4139=
NM_001369.3:c.13815A= MANE Select NP_001360.1:p.Thr4605=