Canonical Allele Identifier: CA359219248
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13792102T>A , CM000667.2:g.13792102T>A GRCh38
NC_000005.9:g.13792211T>A , CM000667.1:g.13792211T>A GRCh37
NC_000005.8:g.13845211T>A NCBI36
NG_013081.1:g.157379A>T
NG_013081.2:g.157379A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.8340A>T MANE Select ENSP00000265104.4:p.Lys2780Asn
ENST00000681290.1:c.8295A>T ENSP00000505288.1:p.Lys2765Asn
ENST00000265104.4:c.8340A>T ENSP00000265104.4:p.Lys2780Asn
NM_001369.2:c.8340A>T NP_001360.1:p.Lys2780Asn
XM_005248262.2:c.8295A>T XP_005248319.1:p.Lys2765Asn
XM_011513990.1:c.8340A>T XP_011512292.1:p.Lys2780Asn
XR_925598.1:n.8547A>T
XM_005248262.3:c.8448A>T XP_005248319.2:p.Lys2816Asn
XM_017009177.1:c.8448A>T XP_016864666.1:p.Lys2816Asn
XM_017009178.1:c.7353A>T XP_016864667.1:p.Lys2451Asn
XM_017009179.2:c.7353A>T XP_016864668.1:p.Lys2451Asn
XM_017009180.1:c.8448A>T XP_016864669.1:p.Lys2816Asn
XM_017009181.1:c.8448A>T XP_016864670.1:p.Lys2816Asn
XM_017009182.1:c.8448A>T XP_016864671.1:p.Lys2816Asn
XM_017009183.1:c.8448A>T XP_016864672.1:p.Lys2816Asn
XM_017009184.1:c.8448A>T XP_016864673.1:p.Lys2816Asn
XM_017009185.1:c.3537A>T XP_016864674.1:p.Lys1179Asn
XM_017009186.1:c.3090A>T XP_016864675.1:p.Lys1030Asn
XM_017009188.1:c.2427A>T XP_016864677.1:p.Lys809Asn
XM_024454388.1:c.7353A>T XP_024310156.1:p.Lys2451Asn
XM_024454389.1:c.6942A>T XP_024310157.1:p.Lys2314Asn
XR_001742034.1:n.8465A>T
XR_001742035.1:n.8465A>T
NM_001369.3:c.8340A>T MANE Select NP_001360.1:p.Lys2780Asn