Canonical Allele Identifier: CA359192547
Community Standard Title: NM_001369.3(DNAH5):c.6962G>A (p.Trp2321Ter)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13817574C>T , CM000667.2:g.13817574C>T GRCh38
NC_000005.9:g.13817683C>T , CM000667.1:g.13817683C>T GRCh37
NC_000005.8:g.13870683C>T NCBI36
NG_013081.1:g.131907G>A
NG_013081.2:g.131907G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.6962G>A MANE Select NP_001360.1:p.Trp2321Ter
ENST00000265104.5:c.6962G>A MANE Select ENSP00000265104.4:p.Trp2321Ter
NM_001369.2:c.6962G>A NP_001360.1:p.Trp2321Ter
ENST00000265104.4:c.6962G>A ENSP00000265104.4:p.Trp2321Ter
ENST00000681290.1:c.6917G>A ENSP00000505288.1:p.Trp2306Ter
ENST00000683090.1:n.1893G>A
XM_005248262.2:c.6917G>A XP_005248319.1:p.Trp2306Ter
XM_005248262.3:c.7070G>A XP_005248319.2:p.Trp2357Ter
XM_011513990.1:c.6962G>A XP_011512292.1:p.Trp2321Ter
XM_017009177.1:c.7070G>A XP_016864666.1:p.Trp2357Ter
XM_017009178.1:c.5975G>A XP_016864667.1:p.Trp1992Ter
XM_017009179.2:c.5975G>A XP_016864668.1:p.Trp1992Ter
XM_017009180.1:c.7070G>A XP_016864669.1:p.Trp2357Ter
XM_017009181.1:c.7070G>A XP_016864670.1:p.Trp2357Ter
XM_017009182.1:c.7070G>A XP_016864671.1:p.Trp2357Ter
XM_017009183.1:c.7070G>A XP_016864672.1:p.Trp2357Ter
XM_017009184.1:c.7070G>A XP_016864673.1:p.Trp2357Ter
XM_017009185.1:c.2159G>A XP_016864674.1:p.Trp720Ter
XM_017009186.1:c.1712G>A XP_016864675.1:p.Trp571Ter
XM_017009187.1:c.7070G>A XP_016864676.1:p.Trp2357Ter
XM_017009188.1:c.1049G>A XP_016864677.1:p.Trp350Ter
XM_024454388.1:c.5975G>A XP_024310156.1:p.Trp1992Ter
XM_024454389.1:c.5564G>A XP_024310157.1:p.Trp1855Ter
XR_001742034.1:n.7087G>A
XR_001742035.1:n.7087G>A
XR_925598.1:n.7169G>A