Canonical Allele Identifier: CA1622423972
Gene: DNAH8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38842578T= , CM000668.2:g.38842578T= GRCh38
NC_000006.11:g.38810354T= , CM000668.1:g.38810354T= GRCh37
NC_000006.10:g.38918332T= NCBI36
NG_041805.1:g.132238T=

Transcript Alleles

HGVS Amino-acid change
ENST00000327475.11:c.4604+73T= MANE Select ENSP00000333363.7:n.4604+73T=
ENST00000327475.10:c.4604+73T= ENSP00000333363.7:n.4604+73T=
ENST00000359357.7:c.3953+73T= ENSP00000352312.3:n.3953+73T=
ENST00000449981.6:c.4604+73T= ENSP00000415331.2:n.4604+73T=
NM_001206927.1:c.4604+73T= NP_001193856.1:n.4604+73T=
XM_011514318.1:c.4541+73T= XP_011512620.1:n.4541+73T=
XM_011514319.1:c.4604+73T= XP_011512621.1:n.4604+73T=
XM_011514320.1:c.4367+73T= XP_011512622.1:n.4367+73T=
XM_011514321.1:c.3953+73T= XP_011512623.1:n.3953+73T=
XM_011514322.1:c.4604+73T= XP_011512624.1:n.4604+73T=
XR_926078.1:n.4721+73T=
NM_001371.3:c.3953+73T= NP_001362.2:n.3953+73T=
XM_011514318.2:c.4541+73T= XP_011512620.1:n.4541+73T=
XM_011514319.2:c.4604+73T= XP_011512621.1:n.4604+73T=
XM_011514320.2:c.4367+73T= XP_011512622.1:n.4367+73T=
XM_017010325.1:c.4604+73T= XP_016865814.1:n.4604+73T=
XM_017010326.1:c.4604+73T= XP_016865815.1:n.4604+73T=
XM_017010327.1:c.4604+73T= XP_016865816.1:n.4604+73T=
XR_001743188.1:n.4725+73T=
XR_926078.2:n.4724+73T=
NM_001206927.2:c.4604+73T= MANE Select NP_001193856.1:n.4604+73T=
NM_001371.4:c.3953+73T= NP_001362.2:n.3953+73T=