Canonical Allele Identifier: CA1528395823
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13691970A= , CM000667.2:g.13691970A= GRCh38
NC_000005.9:g.13692079A= , CM000667.1:g.13692079A= GRCh37
NC_000005.8:g.13745079A= NCBI36
NG_013081.1:g.257511T=
NG_013081.2:g.257511T=

Transcript Alleles

HGVS Amino-acid change
ENST00000683611.1:n.1222T=
ENST00000265104.5:c.*14T= MANE Select ENSP00000265104.4:n.*14T=
ENST00000681290.1:c.*14T= ENSP00000505288.1:n.*14T=
ENST00000265104.4:c.*14T= ENSP00000265104.4:n.*14T=
NM_001369.2:c.*14T= NP_001360.1:n.*14T=
XM_005248262.2:c.*14T= XP_005248319.1:n.*14T=
XM_005248262.3:c.*14T= XP_005248319.2:n.*14T=
XM_017009177.1:c.*14T= XP_016864666.1:n.*14T=
XM_017009178.1:c.*14T= XP_016864667.1:n.*14T=
XM_017009179.2:c.*14T= XP_016864668.1:n.*14T=
XM_017009185.1:c.*14T= XP_016864674.1:n.*14T=
XM_017009186.1:c.*14T= XP_016864675.1:n.*14T=
XM_017009188.1:c.*14T= XP_016864677.1:n.*14T=
XM_024454388.1:c.*14T= XP_024310156.1:n.*14T=
XM_024454389.1:c.*14T= XP_024310157.1:n.*14T=
NM_001369.3:c.*14T= MANE Select NP_001360.1:n.*14T=