Canonical Allele Identifier: CA1528407082
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13717515T= , CM000667.2:g.13717515T= GRCh38
NC_000005.9:g.13717624T= , CM000667.1:g.13717624T= GRCh37
NC_000005.8:g.13770624T= NCBI36
NG_013081.1:g.231966A=
NG_013081.2:g.231966A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.12505A= MANE Select ENSP00000265104.4:p.Ser4169=
ENST00000681290.1:c.12460A= ENSP00000505288.1:p.Ser4154=
ENST00000265104.4:c.12505A= ENSP00000265104.4:p.Ser4169=
NM_001369.2:c.12505A= NP_001360.1:p.Ser4169=
XM_005248262.2:c.12460A= XP_005248319.1:p.Ser4154=
XM_005248262.3:c.12613A= XP_005248319.2:p.Ser4205=
XM_017009177.1:c.12613A= XP_016864666.1:p.Ser4205=
XM_017009178.1:c.11518A= XP_016864667.1:p.Ser3840=
XM_017009179.2:c.11518A= XP_016864668.1:p.Ser3840=
XM_017009180.1:c.12613A= XP_016864669.1:p.Ser4205=
XM_017009185.1:c.7702A= XP_016864674.1:p.Ser2568=
XM_017009186.1:c.7255A= XP_016864675.1:p.Ser2419=
XM_017009188.1:c.6592A= XP_016864677.1:p.Ser2198=
XM_024454388.1:c.11518A= XP_024310156.1:p.Ser3840=
XM_024454389.1:c.11107A= XP_024310157.1:p.Ser3703=
NM_001369.3:c.12505A= MANE Select NP_001360.1:p.Ser4169=