Canonical Allele Identifier: CA137579827

Gene: DNAH8 DNAH8-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.38917924G>A , CM000668.2:g.38917924G>A	GRCh38
NC_000006.11:g.38885700G>A , CM000668.1:g.38885700G>A	GRCh37
NC_000006.10:g.38993678G>A	NCBI36
NG_041805.1:g.207584G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001206927.2:c.10309-1G>A (DNAH8) MANE Select	NP_001193856.1:n.10309-1G>A
ENST00000327475.11:c.10309-1G>A (DNAH8) MANE Select	ENSP00000333363.7:n.10309-1G>A
NM_001206927.1:c.10309-1G>A (DNAH8)	NP_001193856.1:n.10309-1G>A
NM_001371.3:c.9658-1G>A (DNAH8)	NP_001362.2:n.9658-1G>A
NM_001371.4:c.9658-1G>A (DNAH8)	NP_001362.2:n.9658-1G>A
NR_038401.1:n.782+5161C>T (DNAH8-AS1)
ENST00000327475.10:c.10309-1G>A (DNAH8)	ENSP00000333363.7:n.10309-1G>A
ENST00000359357.7:c.9658-1G>A (DNAH8)	ENSP00000352312.3:n.9658-1G>A
ENST00000449981.6:c.10309-1G>A (DNAH8)	ENSP00000415331.2:n.10309-1G>A
XM_011514318.1:c.10246-1G>A (DNAH8)	XP_011512620.1:n.10246-1G>A
XM_011514318.2:c.10246-1G>A (DNAH8)	XP_011512620.1:n.10246-1G>A
XM_011514319.1:c.10201-1G>A (DNAH8)	XP_011512621.1:n.10201-1G>A
XM_011514319.2:c.10201-1G>A (DNAH8)	XP_011512621.1:n.10201-1G>A
XM_011514320.1:c.10072-1G>A (DNAH8)	XP_011512622.1:n.10072-1G>A
XM_011514320.2:c.10072-1G>A (DNAH8)	XP_011512622.1:n.10072-1G>A
XM_011514321.1:c.9658-1G>A (DNAH8)	XP_011512623.1:n.9658-1G>A
XM_017010325.1:c.10309-1G>A (DNAH8)	XP_016865814.1:n.10309-1G>A
XM_017010326.1:c.10309-1G>A (DNAH8)	XP_016865815.1:n.10309-1G>A
XR_926078.1:n.10426-1G>A (DNAH8)
XR_926078.2:n.10429-1G>A (DNAH8)