Canonical Allele Identifier: CA3202908
Community Standard Title: NM_001369.3(DNAH5):c.8059A>G (p.Asn2687Asp)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13793680T>C , CM000667.2:g.13793680T>C GRCh38
NC_000005.9:g.13793789T>C , CM000667.1:g.13793789T>C GRCh37
NC_000005.8:g.13846789T>C NCBI36
NG_013081.1:g.155801A>G
NG_013081.2:g.155801A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.8059A>G MANE Select NP_001360.1:p.Asn2687Asp
ENST00000265104.5:c.8059A>G MANE Select ENSP00000265104.4:p.Asn2687Asp
NM_001369.2:c.8059A>G NP_001360.1:p.Asn2687Asp
ENST00000265104.4:c.8059A>G ENSP00000265104.4:p.Asn2687Asp
ENST00000681290.1:c.8014A>G ENSP00000505288.1:p.Asn2672Asp
XM_005248262.2:c.8014A>G XP_005248319.1:p.Asn2672Asp
XM_005248262.3:c.8167A>G XP_005248319.2:p.Asn2723Asp
XM_011513990.1:c.8059A>G XP_011512292.1:p.Asn2687Asp
XM_017009177.1:c.8167A>G XP_016864666.1:p.Asn2723Asp
XM_017009178.1:c.7072A>G XP_016864667.1:p.Asn2358Asp
XM_017009179.2:c.7072A>G XP_016864668.1:p.Asn2358Asp
XM_017009180.1:c.8167A>G XP_016864669.1:p.Asn2723Asp
XM_017009181.1:c.8167A>G XP_016864670.1:p.Asn2723Asp
XM_017009182.1:c.8167A>G XP_016864671.1:p.Asn2723Asp
XM_017009183.1:c.8167A>G XP_016864672.1:p.Asn2723Asp
XM_017009184.1:c.8167A>G XP_016864673.1:p.Asn2723Asp
XM_017009185.1:c.3256A>G XP_016864674.1:p.Asn1086Asp
XM_017009186.1:c.2809A>G XP_016864675.1:p.Asn937Asp
XM_017009188.1:c.2146A>G XP_016864677.1:p.Asn716Asp
XM_024454388.1:c.7072A>G XP_024310156.1:p.Asn2358Asp
XM_024454389.1:c.6661A>G XP_024310157.1:p.Asn2221Asp
XR_001742034.1:n.8184A>G
XR_001742035.1:n.8184A>G
XR_925598.1:n.8266A>G