Canonical Allele Identifier: CA1528422963
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13752257G= , CM000667.2:g.13752257G= GRCh38
NC_000005.9:g.13752366G= , CM000667.1:g.13752366G= GRCh37
NC_000005.8:g.13805366G= NCBI36
NG_013081.1:g.197224C=
NG_013081.2:g.197224C=

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.10905C= MANE Select ENSP00000265104.4:p.Asn3635=
ENST00000681290.1:c.10860C= ENSP00000505288.1:p.Asn3620=
ENST00000265104.4:c.10905C= ENSP00000265104.4:p.Asn3635=
NM_001369.2:c.10905C= NP_001360.1:p.Asn3635=
XM_005248262.2:c.10860C= XP_005248319.1:p.Asn3620=
XM_005248262.3:c.11013C= XP_005248319.2:p.Asn3671=
XM_017009177.1:c.11013C= XP_016864666.1:p.Asn3671=
XM_017009178.1:c.9918C= XP_016864667.1:p.Asn3306=
XM_017009179.2:c.9918C= XP_016864668.1:p.Asn3306=
XM_017009180.1:c.11013C= XP_016864669.1:p.Asn3671=
XM_017009181.1:c.11013C= XP_016864670.1:p.Asn3671=
XM_017009182.1:c.11013C= XP_016864671.1:p.Asn3671=
XM_017009185.1:c.6102C= XP_016864674.1:p.Asn2034=
XM_017009186.1:c.5655C= XP_016864675.1:p.Asn1885=
XM_017009188.1:c.4992C= XP_016864677.1:p.Asn1664=
XM_024454388.1:c.9918C= XP_024310156.1:p.Asn3306=
XM_024454389.1:c.9507C= XP_024310157.1:p.Asn3169=
NM_001369.3:c.10905C= MANE Select NP_001360.1:p.Asn3635=