Canonical Allele Identifier: CA3791134

Gene: DNAH8 DNAH8-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.38938012C>T , CM000668.2:g.38938012C>T	GRCh38
NC_000006.11:g.38905788C>T , CM000668.1:g.38905788C>T	GRCh37
NC_000006.10:g.39013766C>T	NCBI36
NG_041805.1:g.227672C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001206927.2:c.11602C>T (DNAH8) MANE Select	NP_001193856.1:p.Arg3868Ter
ENST00000327475.11:c.11602C>T (DNAH8) MANE Select	ENSP00000333363.7:p.Arg3868Ter
NM_001206927.1:c.11602C>T (DNAH8)	NP_001193856.1:p.Arg3868Ter
NM_001371.3:c.10951C>T (DNAH8)	NP_001362.2:p.Arg3651Ter
NM_001371.4:c.10951C>T (DNAH8)	NP_001362.2:p.Arg3651Ter
NR_038401.1:n.61-1620G>A (DNAH8-AS1)
ENST00000327475.10:c.11602C>T (DNAH8)	ENSP00000333363.7:p.Arg3868Ter
ENST00000359357.7:c.10951C>T (DNAH8)	ENSP00000352312.3:p.Arg3651Ter
ENST00000449981.6:c.11602C>T (DNAH8)	ENSP00000415331.2:p.Arg3868Ter
XM_011514318.1:c.11539C>T (DNAH8)	XP_011512620.1:p.Arg3847Ter
XM_011514318.2:c.11539C>T (DNAH8)	XP_011512620.1:p.Arg3847Ter
XM_011514319.1:c.11494C>T (DNAH8)	XP_011512621.1:p.Arg3832Ter
XM_011514319.2:c.11494C>T (DNAH8)	XP_011512621.1:p.Arg3832Ter
XM_011514320.1:c.11365C>T (DNAH8)	XP_011512622.1:p.Arg3789Ter
XM_011514320.2:c.11365C>T (DNAH8)	XP_011512622.1:p.Arg3789Ter
XM_011514321.1:c.10951C>T (DNAH8)	XP_011512623.1:p.Arg3651Ter
XM_017010325.1:c.11602C>T (DNAH8)	XP_016865814.1:p.Arg3868Ter
XM_017010326.1:c.11602C>T (DNAH8)	XP_016865815.1:p.Arg3868Ter
XR_926078.1:n.11719C>T (DNAH8)
XR_926078.2:n.11722C>T (DNAH8)