Canonical Allele Identifier: CA3789403

Gene: DNAH8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.38852754G>C , CM000668.2:g.38852754G>C	GRCh38
NC_000006.11:g.38820530G>C , CM000668.1:g.38820530G>C	GRCh37
NC_000006.10:g.38928508G>C	NCBI36
NG_041805.1:g.142414G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001206927.2:c.5527G>C MANE Select	NP_001193856.1:p.Asp1843His
ENST00000327475.11:c.5527G>C MANE Select	ENSP00000333363.7:p.Asp1843His
NM_001206927.1:c.5527G>C	NP_001193856.1:p.Asp1843His
NM_001371.3:c.4876G>C	NP_001362.2:p.Asp1626His
NM_001371.4:c.4876G>C	NP_001362.2:p.Asp1626His
ENST00000327475.10:c.5527G>C	ENSP00000333363.7:p.Asp1843His
ENST00000359357.7:c.4876G>C	ENSP00000352312.3:p.Asp1626His
ENST00000449981.6:c.5527G>C	ENSP00000415331.2:p.Asp1843His
XM_011514318.1:c.5464G>C	XP_011512620.1:p.Asp1822His
XM_011514318.2:c.5464G>C	XP_011512620.1:p.Asp1822His
XM_011514319.1:c.5527G>C	XP_011512621.1:p.Asp1843His
XM_011514319.2:c.5527G>C	XP_011512621.1:p.Asp1843His
XM_011514320.1:c.5290G>C	XP_011512622.1:p.Asp1764His
XM_011514320.2:c.5290G>C	XP_011512622.1:p.Asp1764His
XM_011514321.1:c.4876G>C	XP_011512623.1:p.Asp1626His
XM_011514322.1:c.5527G>C	XP_011512624.1:p.Asp1843His
XM_017010325.1:c.5527G>C	XP_016865814.1:p.Asp1843His
XM_017010326.1:c.5527G>C	XP_016865815.1:p.Asp1843His
XM_017010327.1:c.5527G>C	XP_016865816.1:p.Asp1843His
XR_001743188.1:n.5648G>C
XR_926078.1:n.5644G>C
XR_926078.2:n.5647G>C