Canonical Allele Identifier: CA1980452050

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036389A= , CM000673.2:g.68036389A=	GRCh38
NC_000011.9:g.67803856A= , CM000673.1:g.67803856A=	GRCh37
NC_000011.8:g.67560432A=	NCBI36
NG_007878.1:g.2374A= , LRG_115:g.2374A=
NG_017040.1:g.10773A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.501+8A= MANE Select	ENSP00000315774.5:n.501+8A=
ENST00000313468.9:c.501+8A=	ENSP00000315774.5:n.501+8A=
ENST00000524810.5:c.433+8A=
ENST00000526339.5:c.501+8A=	ENSP00000436287.1:n.501+8A=
ENST00000526446.5:c.*556+8A=	ENSP00000433645.1:n.*556+8A=
ENST00000528492.1:c.63+8A=	ENSP00000432848.1:n.63+8A=
ENST00000531282.1:n.353+8A=
NM_002496.3:c.501+8A=	NP_002487.1:n.501+8A=
XM_005274013.1:c.501+8A=	XP_005274070.1:n.501+8A=
XM_005274014.1:c.501+8A=	XP_005274071.1:n.501+8A=
XM_005274015.1:c.381+8A=	XP_005274072.1:n.381+8A=
XM_011545053.1:c.501+8A=	XP_011543355.1:n.501+8A=
NM_002496.4:c.501+8A= MANE Select	NP_002487.1:n.501+8A=