Canonical Allele Identifier: CA1980451840

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036261C= , CM000673.2:g.68036261C=	GRCh38
NC_000011.9:g.67803728C= , CM000673.1:g.67803728C=	GRCh37
NC_000011.8:g.67560304C=	NCBI36
NG_007878.1:g.2246C= , LRG_115:g.2246C=
NG_017040.1:g.10645C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.381C= MANE Select	ENSP00000315774.5:p.Thr127=
ENST00000313468.9:c.381C=	ENSP00000315774.5:p.Thr127=
ENST00000524810.5:c.313C=
ENST00000525419.5:c.327C=	ENSP00000433521.1:p.Thr109=
ENST00000526339.5:c.381C=	ENSP00000436287.1:p.Thr127=
ENST00000526446.5:c.*436C=	ENSP00000433645.1:n.*436C=
ENST00000526542.1:n.332C=
ENST00000528492.1:c.-58C=	ENSP00000432848.1:n.-58C=
ENST00000531282.1:n.233C=
NM_002496.3:c.381C=	NP_002487.1:p.Thr127=
XM_005274013.1:c.381C=	XP_005274070.1:p.Thr127=
XM_005274014.1:c.381C=	XP_005274071.1:p.Thr127=
XM_005274015.1:c.261C=	XP_005274072.1:p.Thr87=
XM_011545053.1:c.381C=	XP_011543355.1:p.Thr127=
NM_002496.4:c.381C= MANE Select	NP_002487.1:p.Thr127=