Canonical Allele Identifier: CA359231541
Community Standard Title: NM_001369.3(DNAH5):c.7574G>A (p.Gly2525Glu)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13810094C>T , CM000667.2:g.13810094C>T GRCh38
NC_000005.9:g.13810203C>T , CM000667.1:g.13810203C>T GRCh37
NC_000005.8:g.13863203C>T NCBI36
NG_013081.1:g.139387G>A
NG_013081.2:g.139387G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.7574G>A MANE Select NP_001360.1:p.Gly2525Glu
ENST00000265104.5:c.7574G>A MANE Select ENSP00000265104.4:p.Gly2525Glu
NM_001369.2:c.7574G>A NP_001360.1:p.Gly2525Glu
ENST00000265104.4:c.7574G>A ENSP00000265104.4:p.Gly2525Glu
ENST00000512443.1:n.430G>A
ENST00000681290.1:c.7529G>A ENSP00000505288.1:p.Gly2510Glu
XM_005248262.2:c.7529G>A XP_005248319.1:p.Gly2510Glu
XM_005248262.3:c.7682G>A XP_005248319.2:p.Gly2561Glu
XM_011513990.1:c.7574G>A XP_011512292.1:p.Gly2525Glu
XM_017009177.1:c.7682G>A XP_016864666.1:p.Gly2561Glu
XM_017009178.1:c.6587G>A XP_016864667.1:p.Gly2196Glu
XM_017009179.2:c.6587G>A XP_016864668.1:p.Gly2196Glu
XM_017009180.1:c.7682G>A XP_016864669.1:p.Gly2561Glu
XM_017009181.1:c.7682G>A XP_016864670.1:p.Gly2561Glu
XM_017009182.1:c.7682G>A XP_016864671.1:p.Gly2561Glu
XM_017009183.1:c.7682G>A XP_016864672.1:p.Gly2561Glu
XM_017009184.1:c.7682G>A XP_016864673.1:p.Gly2561Glu
XM_017009185.1:c.2771G>A XP_016864674.1:p.Gly924Glu
XM_017009186.1:c.2324G>A XP_016864675.1:p.Gly775Glu
XM_017009187.1:c.7682G>A XP_016864676.1:p.Gly2561Glu
XM_017009188.1:c.1661G>A XP_016864677.1:p.Gly554Glu
XM_024454388.1:c.6587G>A XP_024310156.1:p.Gly2196Glu
XM_024454389.1:c.6176G>A XP_024310157.1:p.Gly2059Glu
XR_001742034.1:n.7699G>A
XR_001742035.1:n.7699G>A
XR_925598.1:n.7781G>A