Canonical Allele Identifier: CA1980451804

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036198T= , CM000673.2:g.68036198T=	GRCh38
NC_000011.9:g.67803665T= , CM000673.1:g.67803665T=	GRCh37
NC_000011.8:g.67560241T=	NCBI36
NG_007878.1:g.2183T= , LRG_115:g.2183T=
NG_017040.1:g.10582T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000313468.10:c.373-55T= MANE Select	ENSP00000315774.5:n.373-55T=
ENST00000313468.9:c.373-55T=	ENSP00000315774.5:n.373-55T=
ENST00000524810.5:c.305-55T=
ENST00000525419.5:c.319-55T=	ENSP00000433521.1:n.319-55T=
ENST00000526339.5:c.373-55T=	ENSP00000436287.1:n.373-55T=
ENST00000526446.5:c.*428-55T=	ENSP00000433645.1:n.*428-55T=
ENST00000526542.1:n.324-55T=
ENST00000528492.1:c.-66-55T=	ENSP00000432848.1:n.-66-55T=
ENST00000531282.1:n.170T=
NM_002496.3:c.373-55T=	NP_002487.1:n.373-55T=
XM_005274013.1:c.373-55T=	XP_005274070.1:n.373-55T=
XM_005274014.1:c.373-55T=	XP_005274071.1:n.373-55T=
XM_005274015.1:c.253-55T=	XP_005274072.1:n.253-55T=
XM_011545053.1:c.373-55T=	XP_011543355.1:n.373-55T=
NM_002496.4:c.373-55T= MANE Select	NP_002487.1:n.373-55T=