Canonical Allele Identifier: CA359190171
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13876770T>C , CM000667.2:g.13876770T>C GRCh38
NC_000005.9:g.13876879T>C , CM000667.1:g.13876879T>C GRCh37
NC_000005.8:g.13929879T>C NCBI36
NG_013081.1:g.72711A>G
NG_013081.2:g.72711A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.3310A>G MANE Select ENSP00000265104.4:p.Lys1104Glu
ENST00000681290.1:c.3265A>G ENSP00000505288.1:p.Lys1089Glu
ENST00000265104.4:c.3310A>G ENSP00000265104.4:p.Lys1104Glu
NM_001369.2:c.3310A>G NP_001360.1:p.Lys1104Glu
XM_005248262.2:c.3265A>G XP_005248319.1:p.Lys1089Glu
XM_011513990.1:c.3310A>G XP_011512292.1:p.Lys1104Glu
XR_925598.1:n.3517A>G
XM_005248262.3:c.3418A>G XP_005248319.2:p.Lys1140Glu
XM_017009177.1:c.3418A>G XP_016864666.1:p.Lys1140Glu
XM_017009178.1:c.2323A>G XP_016864667.1:p.Lys775Glu
XM_017009179.2:c.2323A>G XP_016864668.1:p.Lys775Glu
XM_017009180.1:c.3418A>G XP_016864669.1:p.Lys1140Glu
XM_017009181.1:c.3418A>G XP_016864670.1:p.Lys1140Glu
XM_017009182.1:c.3418A>G XP_016864671.1:p.Lys1140Glu
XM_017009183.1:c.3418A>G XP_016864672.1:p.Lys1140Glu
XM_017009184.1:c.3418A>G XP_016864673.1:p.Lys1140Glu
XM_017009187.1:c.3418A>G XP_016864676.1:p.Lys1140Glu
XM_024454388.1:c.2323A>G XP_024310156.1:p.Lys775Glu
XM_024454389.1:c.1912A>G XP_024310157.1:p.Lys638Glu
XR_001742034.1:n.3435A>G
XR_001742035.1:n.3435A>G
NM_001369.3:c.3310A>G MANE Select NP_001360.1:p.Lys1104Glu