Canonical Allele Identifier: CA364011561

Gene: DNAH8 DNAH8-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.38923056A>G , CM000668.2:g.38923056A>G	GRCh38
NC_000006.11:g.38890832A>G , CM000668.1:g.38890832A>G	GRCh37
NC_000006.10:g.38998810A>G	NCBI36
NG_041805.1:g.212716A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001206927.2:c.10663-2A>G (DNAH8) MANE Select	NP_001193856.1:n.10663-2A>G
ENST00000327475.11:c.10663-2A>G (DNAH8) MANE Select	ENSP00000333363.7:n.10663-2A>G
NM_001206927.1:c.10663-2A>G (DNAH8)	NP_001193856.1:n.10663-2A>G
NM_001371.3:c.10012-2A>G (DNAH8)	NP_001362.2:n.10012-2A>G
NM_001371.4:c.10012-2A>G (DNAH8)	NP_001362.2:n.10012-2A>G
NR_038401.1:n.782+29T>C (DNAH8-AS1)
ENST00000327475.10:c.10663-2A>G (DNAH8)	ENSP00000333363.7:n.10663-2A>G
ENST00000359357.7:c.10012-2A>G (DNAH8)	ENSP00000352312.3:n.10012-2A>G
ENST00000449981.6:c.10663-2A>G (DNAH8)	ENSP00000415331.2:n.10663-2A>G
XM_011514318.1:c.10600-2A>G (DNAH8)	XP_011512620.1:n.10600-2A>G
XM_011514318.2:c.10600-2A>G (DNAH8)	XP_011512620.1:n.10600-2A>G
XM_011514319.1:c.10555-2A>G (DNAH8)	XP_011512621.1:n.10555-2A>G
XM_011514319.2:c.10555-2A>G (DNAH8)	XP_011512621.1:n.10555-2A>G
XM_011514320.1:c.10426-2A>G (DNAH8)	XP_011512622.1:n.10426-2A>G
XM_011514320.2:c.10426-2A>G (DNAH8)	XP_011512622.1:n.10426-2A>G
XM_011514321.1:c.10012-2A>G (DNAH8)	XP_011512623.1:n.10012-2A>G
XM_017010325.1:c.10663-2A>G (DNAH8)	XP_016865814.1:n.10663-2A>G
XM_017010326.1:c.10663-2A>G (DNAH8)	XP_016865815.1:n.10663-2A>G
XR_926078.1:n.10780-2A>G (DNAH8)
XR_926078.2:n.10783-2A>G (DNAH8)