Canonical Allele Identifier: CA363990767

Gene: DNAH8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.38790323T>A , CM000668.2:g.38790323T>A	GRCh38
NC_000006.11:g.38758099T>A , CM000668.1:g.38758099T>A	GRCh37
NC_000006.10:g.38866077T>A	NCBI36
NG_041805.1:g.79983T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001206927.2:c.2699T>A MANE Select	NP_001193856.1:p.Leu900Ter
ENST00000327475.11:c.2699T>A MANE Select	ENSP00000333363.7:p.Leu900Ter
NM_001206927.1:c.2699T>A	NP_001193856.1:p.Leu900Ter
NM_001371.3:c.2048T>A	NP_001362.2:p.Leu683Ter
NM_001371.4:c.2048T>A	NP_001362.2:p.Leu683Ter
ENST00000327475.10:c.2699T>A	ENSP00000333363.7:p.Leu900Ter
ENST00000359357.7:c.2048T>A	ENSP00000352312.3:p.Leu683Ter
ENST00000449981.6:c.2699T>A	ENSP00000415331.2:p.Leu900Ter
XM_011514318.1:c.2699T>A	XP_011512620.1:p.Leu900Ter
XM_011514318.2:c.2699T>A	XP_011512620.1:p.Leu900Ter
XM_011514319.1:c.2699T>A	XP_011512621.1:p.Leu900Ter
XM_011514319.2:c.2699T>A	XP_011512621.1:p.Leu900Ter
XM_011514320.1:c.2462T>A	XP_011512622.1:p.Leu821Ter
XM_011514320.2:c.2462T>A	XP_011512622.1:p.Leu821Ter
XM_011514321.1:c.2048T>A	XP_011512623.1:p.Leu683Ter
XM_011514322.1:c.2699T>A	XP_011512624.1:p.Leu900Ter
XM_017010325.1:c.2699T>A	XP_016865814.1:p.Leu900Ter
XM_017010326.1:c.2699T>A	XP_016865815.1:p.Leu900Ter
XM_017010327.1:c.2699T>A	XP_016865816.1:p.Leu900Ter
XR_001743188.1:n.2820T>A
XR_926078.1:n.2816T>A
XR_926078.2:n.2819T>A