Canonical Allele Identifier: CA1528476285
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13870746G= , CM000667.2:g.13870746G= GRCh38
NC_000005.9:g.13870855G= , CM000667.1:g.13870855G= GRCh37
NC_000005.8:g.13923855G= NCBI36
NG_013081.1:g.78735C=
NG_013081.2:g.78735C=

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.3834+21C= MANE Select ENSP00000265104.4:n.3834+21C=
ENST00000681290.1:c.3789+21C= ENSP00000505288.1:n.3789+21C=
ENST00000265104.4:c.3834+21C= ENSP00000265104.4:n.3834+21C=
NM_001369.2:c.3834+21C= NP_001360.1:n.3834+21C=
XM_005248262.2:c.3789+21C= XP_005248319.1:n.3789+21C=
XM_011513990.1:c.3834+21C= XP_011512292.1:n.3834+21C=
XR_925598.1:n.4041+21C=
XM_005248262.3:c.3942+21C= XP_005248319.2:n.3942+21C=
XM_017009177.1:c.3942+21C= XP_016864666.1:n.3942+21C=
XM_017009178.1:c.2847+21C= XP_016864667.1:n.2847+21C=
XM_017009179.2:c.2847+21C= XP_016864668.1:n.2847+21C=
XM_017009180.1:c.3942+21C= XP_016864669.1:n.3942+21C=
XM_017009181.1:c.3942+21C= XP_016864670.1:n.3942+21C=
XM_017009182.1:c.3942+21C= XP_016864671.1:n.3942+21C=
XM_017009183.1:c.3942+21C= XP_016864672.1:n.3942+21C=
XM_017009184.1:c.3942+21C= XP_016864673.1:n.3942+21C=
XM_017009187.1:c.3942+21C= XP_016864676.1:n.3942+21C=
XM_024454388.1:c.2847+21C= XP_024310156.1:n.2847+21C=
XM_024454389.1:c.2436+21C= XP_024310157.1:n.2436+21C=
XR_001742034.1:n.3959+21C=
XR_001742035.1:n.3959+21C=
NM_001369.3:c.3834+21C= MANE Select NP_001360.1:n.3834+21C=