Canonical Allele Identifier: CA359202566
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13830661T>G , CM000667.2:g.13830661T>G GRCh38
NC_000005.9:g.13830770T>G , CM000667.1:g.13830770T>G GRCh37
NC_000005.8:g.13883770T>G NCBI36
NG_013081.1:g.118820A>C
NG_013081.2:g.118820A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000683090.1:n.928A>C
ENST00000265104.5:c.5997A>C MANE Select ENSP00000265104.4:p.Lys1999Asn
ENST00000681290.1:c.5952A>C ENSP00000505288.1:p.Lys1984Asn
ENST00000265104.4:c.5997A>C ENSP00000265104.4:p.Lys1999Asn
NM_001369.2:c.5997A>C NP_001360.1:p.Lys1999Asn
XM_005248262.2:c.5952A>C XP_005248319.1:p.Lys1984Asn
XM_011513990.1:c.5997A>C XP_011512292.1:p.Lys1999Asn
XR_925598.1:n.6204A>C
XM_005248262.3:c.6105A>C XP_005248319.2:p.Lys2035Asn
XM_017009177.1:c.6105A>C XP_016864666.1:p.Lys2035Asn
XM_017009178.1:c.5010A>C XP_016864667.1:p.Lys1670Asn
XM_017009179.2:c.5010A>C XP_016864668.1:p.Lys1670Asn
XM_017009180.1:c.6105A>C XP_016864669.1:p.Lys2035Asn
XM_017009181.1:c.6105A>C XP_016864670.1:p.Lys2035Asn
XM_017009182.1:c.6105A>C XP_016864671.1:p.Lys2035Asn
XM_017009183.1:c.6105A>C XP_016864672.1:p.Lys2035Asn
XM_017009184.1:c.6105A>C XP_016864673.1:p.Lys2035Asn
XM_017009185.1:c.1194A>C XP_016864674.1:p.Lys398Asn
XM_017009186.1:c.747A>C XP_016864675.1:p.Lys249Asn
XM_017009187.1:c.6105A>C XP_016864676.1:p.Lys2035Asn
XM_017009188.1:c.84A>C XP_016864677.1:p.Lys28Asn
XM_024454388.1:c.5010A>C XP_024310156.1:p.Lys1670Asn
XM_024454389.1:c.4599A>C XP_024310157.1:p.Lys1533Asn
XR_001742034.1:n.6122A>C
XR_001742035.1:n.6122A>C
NM_001369.3:c.5997A>C MANE Select NP_001360.1:p.Lys1999Asn