Canonical Allele Identifier: CA359231069
Community Standard Title: NM_001369.3(DNAH5):c.7616G>A (p.Trp2539Ter)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13809180C>T , CM000667.2:g.13809180C>T GRCh38
NC_000005.9:g.13809289C>T , CM000667.1:g.13809289C>T GRCh37
NC_000005.8:g.13862289C>T NCBI36
NG_013081.1:g.140301G>A
NG_013081.2:g.140301G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.7616G>A MANE Select NP_001360.1:p.Trp2539Ter
ENST00000265104.5:c.7616G>A MANE Select ENSP00000265104.4:p.Trp2539Ter
NM_001369.2:c.7616G>A NP_001360.1:p.Trp2539Ter
ENST00000265104.4:c.7616G>A ENSP00000265104.4:p.Trp2539Ter
ENST00000512443.1:n.472G>A
ENST00000681290.1:c.7571G>A ENSP00000505288.1:p.Trp2524Ter
XM_005248262.2:c.7571G>A XP_005248319.1:p.Trp2524Ter
XM_005248262.3:c.7724G>A XP_005248319.2:p.Trp2575Ter
XM_011513990.1:c.7616G>A XP_011512292.1:p.Trp2539Ter
XM_017009177.1:c.7724G>A XP_016864666.1:p.Trp2575Ter
XM_017009178.1:c.6629G>A XP_016864667.1:p.Trp2210Ter
XM_017009179.2:c.6629G>A XP_016864668.1:p.Trp2210Ter
XM_017009180.1:c.7724G>A XP_016864669.1:p.Trp2575Ter
XM_017009181.1:c.7724G>A XP_016864670.1:p.Trp2575Ter
XM_017009182.1:c.7724G>A XP_016864671.1:p.Trp2575Ter
XM_017009183.1:c.7724G>A XP_016864672.1:p.Trp2575Ter
XM_017009184.1:c.7724G>A XP_016864673.1:p.Trp2575Ter
XM_017009185.1:c.2813G>A XP_016864674.1:p.Trp938Ter
XM_017009186.1:c.2366G>A XP_016864675.1:p.Trp789Ter
XM_017009187.1:c.7724G>A XP_016864676.1:p.Trp2575Ter
XM_017009188.1:c.1703G>A XP_016864677.1:p.Trp568Ter
XM_024454388.1:c.6629G>A XP_024310156.1:p.Trp2210Ter
XM_024454389.1:c.6218G>A XP_024310157.1:p.Trp2073Ter
XR_001742034.1:n.7741G>A
XR_001742035.1:n.7741G>A
XR_925598.1:n.7823G>A