Canonical Allele Identifier: CA359219278
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13792109T>A , CM000667.2:g.13792109T>A GRCh38
NC_000005.9:g.13792218T>A , CM000667.1:g.13792218T>A GRCh37
NC_000005.8:g.13845218T>A NCBI36
NG_013081.1:g.157372A>T
NG_013081.2:g.157372A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.8333A>T MANE Select ENSP00000265104.4:p.Lys2778Met
ENST00000681290.1:c.8288A>T ENSP00000505288.1:p.Lys2763Met
ENST00000265104.4:c.8333A>T ENSP00000265104.4:p.Lys2778Met
NM_001369.2:c.8333A>T NP_001360.1:p.Lys2778Met
XM_005248262.2:c.8288A>T XP_005248319.1:p.Lys2763Met
XM_011513990.1:c.8333A>T XP_011512292.1:p.Lys2778Met
XR_925598.1:n.8540A>T
XM_005248262.3:c.8441A>T XP_005248319.2:p.Lys2814Met
XM_017009177.1:c.8441A>T XP_016864666.1:p.Lys2814Met
XM_017009178.1:c.7346A>T XP_016864667.1:p.Lys2449Met
XM_017009179.2:c.7346A>T XP_016864668.1:p.Lys2449Met
XM_017009180.1:c.8441A>T XP_016864669.1:p.Lys2814Met
XM_017009181.1:c.8441A>T XP_016864670.1:p.Lys2814Met
XM_017009182.1:c.8441A>T XP_016864671.1:p.Lys2814Met
XM_017009183.1:c.8441A>T XP_016864672.1:p.Lys2814Met
XM_017009184.1:c.8441A>T XP_016864673.1:p.Lys2814Met
XM_017009185.1:c.3530A>T XP_016864674.1:p.Lys1177Met
XM_017009186.1:c.3083A>T XP_016864675.1:p.Lys1028Met
XM_017009188.1:c.2420A>T XP_016864677.1:p.Lys807Met
XM_024454388.1:c.7346A>T XP_024310156.1:p.Lys2449Met
XM_024454389.1:c.6935A>T XP_024310157.1:p.Lys2312Met
XR_001742034.1:n.8458A>T
XR_001742035.1:n.8458A>T
NM_001369.3:c.8333A>T MANE Select NP_001360.1:p.Lys2778Met