Canonical Allele Identifier: CA1528430415
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13769172C= , CM000667.2:g.13769172C= GRCh38
NC_000005.9:g.13769281C= , CM000667.1:g.13769281C= GRCh37
NC_000005.8:g.13822281C= NCBI36
NG_013081.1:g.180309G=
NG_013081.2:g.180309G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9721-36G= MANE Select ENSP00000265104.4:n.9721-36G=
ENST00000681290.1:c.9676-36G= ENSP00000505288.1:n.9676-36G=
ENST00000265104.4:c.9721-36G= ENSP00000265104.4:n.9721-36G=
ENST00000504001.3:n.433-36G=
NM_001369.2:c.9721-36G= NP_001360.1:n.9721-36G=
XM_005248262.2:c.9676-36G= XP_005248319.1:n.9676-36G=
XM_005248262.3:c.9829-36G= XP_005248319.2:n.9829-36G=
XM_017009177.1:c.9829-36G= XP_016864666.1:n.9829-36G=
XM_017009178.1:c.8734-36G= XP_016864667.1:n.8734-36G=
XM_017009179.2:c.8734-36G= XP_016864668.1:n.8734-36G=
XM_017009180.1:c.9829-36G= XP_016864669.1:n.9829-36G=
XM_017009181.1:c.9829-36G= XP_016864670.1:n.9829-36G=
XM_017009182.1:c.9829-36G= XP_016864671.1:n.9829-36G=
XM_017009185.1:c.4918-36G= XP_016864674.1:n.4918-36G=
XM_017009186.1:c.4471-36G= XP_016864675.1:n.4471-36G=
XM_017009188.1:c.3808-36G= XP_016864677.1:n.3808-36G=
XM_024454388.1:c.8734-36G= XP_024310156.1:n.8734-36G=
XM_024454389.1:c.8323-36G= XP_024310157.1:n.8323-36G=
NM_001369.3:c.9721-36G= MANE Select NP_001360.1:n.9721-36G=