Canonical Allele Identifier: CA359230931
Community Standard Title: NM_001369.3(DNAH5):c.7647C>G (p.Tyr2549Ter)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13809149G>C , CM000667.2:g.13809149G>C GRCh38
NC_000005.9:g.13809258G>C , CM000667.1:g.13809258G>C GRCh37
NC_000005.8:g.13862258G>C NCBI36
NG_013081.1:g.140332C>G
NG_013081.2:g.140332C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.7647C>G MANE Select NP_001360.1:p.Tyr2549Ter
ENST00000265104.5:c.7647C>G MANE Select ENSP00000265104.4:p.Tyr2549Ter
NM_001369.2:c.7647C>G NP_001360.1:p.Tyr2549Ter
ENST00000265104.4:c.7647C>G ENSP00000265104.4:p.Tyr2549Ter
ENST00000512443.1:n.503C>G
ENST00000681290.1:c.7602C>G ENSP00000505288.1:p.Tyr2534Ter
XM_005248262.2:c.7602C>G XP_005248319.1:p.Tyr2534Ter
XM_005248262.3:c.7755C>G XP_005248319.2:p.Tyr2585Ter
XM_011513990.1:c.7647C>G XP_011512292.1:p.Tyr2549Ter
XM_017009177.1:c.7755C>G XP_016864666.1:p.Tyr2585Ter
XM_017009178.1:c.6660C>G XP_016864667.1:p.Tyr2220Ter
XM_017009179.2:c.6660C>G XP_016864668.1:p.Tyr2220Ter
XM_017009180.1:c.7755C>G XP_016864669.1:p.Tyr2585Ter
XM_017009181.1:c.7755C>G XP_016864670.1:p.Tyr2585Ter
XM_017009182.1:c.7755C>G XP_016864671.1:p.Tyr2585Ter
XM_017009183.1:c.7755C>G XP_016864672.1:p.Tyr2585Ter
XM_017009184.1:c.7755C>G XP_016864673.1:p.Tyr2585Ter
XM_017009185.1:c.2844C>G XP_016864674.1:p.Tyr948Ter
XM_017009186.1:c.2397C>G XP_016864675.1:p.Tyr799Ter
XM_017009187.1:c.7755C>G XP_016864676.1:p.Tyr2585Ter
XM_017009188.1:c.1734C>G XP_016864677.1:p.Tyr578Ter
XM_024454388.1:c.6660C>G XP_024310156.1:p.Tyr2220Ter
XM_024454389.1:c.6249C>G XP_024310157.1:p.Tyr2083Ter
XR_001742034.1:n.7772C>G
XR_001742035.1:n.7772C>G
XR_925598.1:n.7854C>G