Canonical Allele Identifier: CA1980452365

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036511A= , CM000673.2:g.68036511A=	GRCh38
NC_000011.9:g.67803978A= , CM000673.1:g.67803978A=	GRCh37
NC_000011.8:g.67560554A=	NCBI36
NG_007878.1:g.2496A= , LRG_115:g.2496A=
NG_017040.1:g.10895A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.551A= MANE Select	ENSP00000315774.5:p.Asn184=
ENST00000313468.9:c.551A=	ENSP00000315774.5:p.Asn184=
ENST00000524810.5:c.483A=
ENST00000526339.5:c.551A=	ENSP00000436287.1:p.Asn184=
ENST00000526446.5:c.*606A=	ENSP00000433645.1:n.*606A=
ENST00000528492.1:c.113A=	ENSP00000432848.1:p.Asn38=
ENST00000531282.1:n.403A=
NM_002496.3:c.551A=	NP_002487.1:p.Asn184=
XM_005274013.1:c.551A=	XP_005274070.1:p.Asn184=
XM_005274014.1:c.551A=	XP_005274071.1:p.Asn184=
XM_005274015.1:c.431A=	XP_005274072.1:p.Asn144=
XM_011545053.1:c.551A=	XP_011543355.1:p.Asn184=
NM_002496.4:c.551A= MANE Select	NP_002487.1:p.Asn184=