Canonical Allele Identifier: CA359199550
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13829540G>C , CM000667.2:g.13829540G>C GRCh38
NC_000005.9:g.13829649G>C , CM000667.1:g.13829649G>C GRCh37
NC_000005.8:g.13882649G>C NCBI36
NG_013081.1:g.119941C>G
NG_013081.2:g.119941C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000683090.1:n.1345C>G
ENST00000265104.5:c.6414C>G MANE Select ENSP00000265104.4:p.Tyr2138Ter
ENST00000681290.1:c.6369C>G ENSP00000505288.1:p.Tyr2123Ter
ENST00000265104.4:c.6414C>G ENSP00000265104.4:p.Tyr2138Ter
NM_001369.2:c.6414C>G NP_001360.1:p.Tyr2138Ter
XM_005248262.2:c.6369C>G XP_005248319.1:p.Tyr2123Ter
XM_011513990.1:c.6414C>G XP_011512292.1:p.Tyr2138Ter
XR_925598.1:n.6621C>G
XM_005248262.3:c.6522C>G XP_005248319.2:p.Tyr2174Ter
XM_017009177.1:c.6522C>G XP_016864666.1:p.Tyr2174Ter
XM_017009178.1:c.5427C>G XP_016864667.1:p.Tyr1809Ter
XM_017009179.2:c.5427C>G XP_016864668.1:p.Tyr1809Ter
XM_017009180.1:c.6522C>G XP_016864669.1:p.Tyr2174Ter
XM_017009181.1:c.6522C>G XP_016864670.1:p.Tyr2174Ter
XM_017009182.1:c.6522C>G XP_016864671.1:p.Tyr2174Ter
XM_017009183.1:c.6522C>G XP_016864672.1:p.Tyr2174Ter
XM_017009184.1:c.6522C>G XP_016864673.1:p.Tyr2174Ter
XM_017009185.1:c.1611C>G XP_016864674.1:p.Tyr537Ter
XM_017009186.1:c.1164C>G XP_016864675.1:p.Tyr388Ter
XM_017009187.1:c.6522C>G XP_016864676.1:p.Tyr2174Ter
XM_017009188.1:c.501C>G XP_016864677.1:p.Tyr167Ter
XM_024454388.1:c.5427C>G XP_024310156.1:p.Tyr1809Ter
XM_024454389.1:c.5016C>G XP_024310157.1:p.Tyr1672Ter
XR_001742034.1:n.6539C>G
XR_001742035.1:n.6539C>G
NM_001369.3:c.6414C>G MANE Select NP_001360.1:p.Tyr2138Ter