Canonical Allele Identifier: CA3789343

Gene: DNAH8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.38850418A>T , CM000668.2:g.38850418A>T	GRCh38
NC_000006.11:g.38818194A>T , CM000668.1:g.38818194A>T	GRCh37
NC_000006.10:g.38926172A>T	NCBI36
NG_041805.1:g.140078A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001206927.2:c.5363+4A>T MANE Select	NP_001193856.1:n.5363+4A>T
ENST00000327475.11:c.5363+4A>T MANE Select	ENSP00000333363.7:n.5363+4A>T
NM_001206927.1:c.5363+4A>T	NP_001193856.1:n.5363+4A>T
NM_001371.3:c.4712+4A>T	NP_001362.2:n.4712+4A>T
NM_001371.4:c.4712+4A>T	NP_001362.2:n.4712+4A>T
ENST00000327475.10:c.5363+4A>T	ENSP00000333363.7:n.5363+4A>T
ENST00000359357.7:c.4712+4A>T	ENSP00000352312.3:n.4712+4A>T
ENST00000449981.6:c.5363+4A>T	ENSP00000415331.2:n.5363+4A>T
XM_011514318.1:c.5300+4A>T	XP_011512620.1:n.5300+4A>T
XM_011514318.2:c.5300+4A>T	XP_011512620.1:n.5300+4A>T
XM_011514319.1:c.5363+4A>T	XP_011512621.1:n.5363+4A>T
XM_011514319.2:c.5363+4A>T	XP_011512621.1:n.5363+4A>T
XM_011514320.1:c.5126+4A>T	XP_011512622.1:n.5126+4A>T
XM_011514320.2:c.5126+4A>T	XP_011512622.1:n.5126+4A>T
XM_011514321.1:c.4712+4A>T	XP_011512623.1:n.4712+4A>T
XM_011514322.1:c.5363+4A>T	XP_011512624.1:n.5363+4A>T
XM_017010325.1:c.5363+4A>T	XP_016865814.1:n.5363+4A>T
XM_017010326.1:c.5363+4A>T	XP_016865815.1:n.5363+4A>T
XM_017010327.1:c.5363+4A>T	XP_016865816.1:n.5363+4A>T
XR_001743188.1:n.5484+4A>T
XR_926078.1:n.5480+4A>T
XR_926078.2:n.5483+4A>T