Canonical Allele Identifier: CA450134067

Gene: DNAH8

Linked Data

• gnomAD v4: 6-38842663-A-G
• MyVariant Identifiers: chr6:g.38810439A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.38842663A>G , CM000668.2:g.38842663A>G	GRCh38
NC_000006.11:g.38810439A>G , CM000668.1:g.38810439A>G	GRCh37
NC_000006.10:g.38918417A>G	NCBI36
NG_041805.1:g.132323A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327475.11:c.4605A>G MANE Select	ENSP00000333363.7:p.Arg1535=
ENST00000327475.10:c.4605A>G	ENSP00000333363.7:p.Arg1535=
ENST00000359357.7:c.3954A>G	ENSP00000352312.3:p.Arg1318=
ENST00000449981.6:c.4605A>G	ENSP00000415331.2:p.Arg1535=
NM_001206927.1:c.4605A>G	NP_001193856.1:p.Arg1535=
XM_011514318.1:c.4542A>G	XP_011512620.1:p.Arg1514=
XM_011514319.1:c.4605A>G	XP_011512621.1:p.Arg1535=
XM_011514320.1:c.4368A>G	XP_011512622.1:p.Arg1456=
XM_011514321.1:c.3954A>G	XP_011512623.1:p.Arg1318=
XM_011514322.1:c.4605A>G	XP_011512624.1:p.Arg1535=
XR_926078.1:n.4722A>G
NM_001371.3:c.3954A>G	NP_001362.2:p.Arg1318=
XM_011514318.2:c.4542A>G	XP_011512620.1:p.Arg1514=
XM_011514319.2:c.4605A>G	XP_011512621.1:p.Arg1535=
XM_011514320.2:c.4368A>G	XP_011512622.1:p.Arg1456=
XM_017010325.1:c.4605A>G	XP_016865814.1:p.Arg1535=
XM_017010326.1:c.4605A>G	XP_016865815.1:p.Arg1535=
XM_017010327.1:c.4605A>G	XP_016865816.1:p.Arg1535=
XR_001743188.1:n.4726A>G
XR_926078.2:n.4725A>G
NM_001206927.2:c.4605A>G MANE Select	NP_001193856.1:p.Arg1535=
NM_001371.4:c.3954A>G	NP_001362.2:p.Arg1318=