Canonical Allele Identifier: CA1622424084
Gene: DNAH8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38842682G= , CM000668.2:g.38842682G= GRCh38
NC_000006.11:g.38810458G= , CM000668.1:g.38810458G= GRCh37
NC_000006.10:g.38918436G= NCBI36
NG_041805.1:g.132342G=

Transcript Alleles

HGVS Amino-acid change
ENST00000327475.11:c.4624G= MANE Select ENSP00000333363.7:p.Gly1542=
ENST00000327475.10:c.4624G= ENSP00000333363.7:p.Gly1542=
ENST00000359357.7:c.3973G= ENSP00000352312.3:p.Gly1325=
ENST00000449981.6:c.4624G= ENSP00000415331.2:p.Gly1542=
NM_001206927.1:c.4624G= NP_001193856.1:p.Gly1542=
XM_011514318.1:c.4561G= XP_011512620.1:p.Gly1521=
XM_011514319.1:c.4624G= XP_011512621.1:p.Gly1542=
XM_011514320.1:c.4387G= XP_011512622.1:p.Gly1463=
XM_011514321.1:c.3973G= XP_011512623.1:p.Gly1325=
XM_011514322.1:c.4624G= XP_011512624.1:p.Gly1542=
XR_926078.1:n.4741G=
NM_001371.3:c.3973G= NP_001362.2:p.Gly1325=
XM_011514318.2:c.4561G= XP_011512620.1:p.Gly1521=
XM_011514319.2:c.4624G= XP_011512621.1:p.Gly1542=
XM_011514320.2:c.4387G= XP_011512622.1:p.Gly1463=
XM_017010325.1:c.4624G= XP_016865814.1:p.Gly1542=
XM_017010326.1:c.4624G= XP_016865815.1:p.Gly1542=
XM_017010327.1:c.4624G= XP_016865816.1:p.Gly1542=
XR_001743188.1:n.4745G=
XR_926078.2:n.4744G=
NM_001206927.2:c.4624G= MANE Select NP_001193856.1:p.Gly1542=
NM_001371.4:c.3973G= NP_001362.2:p.Gly1325=