Canonical Allele Identifier: CA364003379

Gene: DNAH8

Linked Data

• MyVariant Identifiers: chr6:g.38810447A>T (hg19) ; chr6:g.38842671A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.38842671A>T , CM000668.2:g.38842671A>T	GRCh38
NC_000006.11:g.38810447A>T , CM000668.1:g.38810447A>T	GRCh37
NC_000006.10:g.38918425A>T	NCBI36
NG_041805.1:g.132331A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000327475.11:c.4613A>T MANE Select	ENSP00000333363.7:p.Lys1538Ile
ENST00000327475.10:c.4613A>T	ENSP00000333363.7:p.Lys1538Ile
ENST00000359357.7:c.3962A>T	ENSP00000352312.3:p.Lys1321Ile
ENST00000449981.6:c.4613A>T	ENSP00000415331.2:p.Lys1538Ile
NM_001206927.1:c.4613A>T	NP_001193856.1:p.Lys1538Ile
XM_011514318.1:c.4550A>T	XP_011512620.1:p.Lys1517Ile
XM_011514319.1:c.4613A>T	XP_011512621.1:p.Lys1538Ile
XM_011514320.1:c.4376A>T	XP_011512622.1:p.Lys1459Ile
XM_011514321.1:c.3962A>T	XP_011512623.1:p.Lys1321Ile
XM_011514322.1:c.4613A>T	XP_011512624.1:p.Lys1538Ile
XR_926078.1:n.4730A>T
NM_001371.3:c.3962A>T	NP_001362.2:p.Lys1321Ile
XM_011514318.2:c.4550A>T	XP_011512620.1:p.Lys1517Ile
XM_011514319.2:c.4613A>T	XP_011512621.1:p.Lys1538Ile
XM_011514320.2:c.4376A>T	XP_011512622.1:p.Lys1459Ile
XM_017010325.1:c.4613A>T	XP_016865814.1:p.Lys1538Ile
XM_017010326.1:c.4613A>T	XP_016865815.1:p.Lys1538Ile
XM_017010327.1:c.4613A>T	XP_016865816.1:p.Lys1538Ile
XR_001743188.1:n.4734A>T
XR_926078.2:n.4733A>T
NM_001206927.2:c.4613A>T MANE Select	NP_001193856.1:p.Lys1538Ile
NM_001371.4:c.3962A>T	NP_001362.2:p.Lys1321Ile