Canonical Allele Identifier: CA359210931
Community Standard Title: NM_001369.3(DNAH5):c.9022G>A (p.Gly3008Arg)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13777285C>T , CM000667.2:g.13777285C>T GRCh38
NC_000005.9:g.13777394C>T , CM000667.1:g.13777394C>T GRCh37
NC_000005.8:g.13830394C>T NCBI36
NG_013081.1:g.172196G>A
NG_013081.2:g.172196G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.9022G>A MANE Select NP_001360.1:p.Gly3008Arg
ENST00000265104.5:c.9022G>A MANE Select ENSP00000265104.4:p.Gly3008Arg
NM_001369.2:c.9022G>A NP_001360.1:p.Gly3008Arg
ENST00000265104.4:c.9022G>A ENSP00000265104.4:p.Gly3008Arg
ENST00000681290.1:c.8977G>A ENSP00000505288.1:p.Gly2993Arg
XM_005248262.2:c.8977G>A XP_005248319.1:p.Gly2993Arg
XM_005248262.3:c.9130G>A XP_005248319.2:p.Gly3044Arg
XM_011513990.1:c.9022G>A XP_011512292.1:p.Gly3008Arg
XM_017009177.1:c.9130G>A XP_016864666.1:p.Gly3044Arg
XM_017009178.1:c.8035G>A XP_016864667.1:p.Gly2679Arg
XM_017009179.2:c.8035G>A XP_016864668.1:p.Gly2679Arg
XM_017009180.1:c.9130G>A XP_016864669.1:p.Gly3044Arg
XM_017009181.1:c.9130G>A XP_016864670.1:p.Gly3044Arg
XM_017009182.1:c.9130G>A XP_016864671.1:p.Gly3044Arg
XM_017009183.1:c.9130G>A XP_016864672.1:p.Gly3044Arg
XM_017009184.1:c.9130G>A XP_016864673.1:p.Gly3044Arg
XM_017009185.1:c.4219G>A XP_016864674.1:p.Gly1407Arg
XM_017009186.1:c.3772G>A XP_016864675.1:p.Gly1258Arg
XM_017009188.1:c.3109G>A XP_016864677.1:p.Gly1037Arg
XM_024454388.1:c.8035G>A XP_024310156.1:p.Gly2679Arg
XM_024454389.1:c.7624G>A XP_024310157.1:p.Gly2542Arg
XR_001742034.1:n.9016G>A
XR_001742035.1:n.9016G>A
XR_925598.1:n.9098G>A