Canonical Allele Identifier: CA381569128

Gene: NDUFS8

Linked Data

• MyVariant Identifiers: chr11:g.67803784A>C (hg19) ; chr11:g.68036317A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036317A>C , CM000673.2:g.68036317A>C	GRCh38
NC_000011.9:g.67803784A>C , CM000673.1:g.67803784A>C	GRCh37
NC_000011.8:g.67560360A>C	NCBI36
NG_007878.1:g.2302A>C , LRG_115:g.2302A>C
NG_017040.1:g.10701A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.437A>C MANE Select	ENSP00000315774.5:p.Asp146Ala
ENST00000313468.9:c.437A>C	ENSP00000315774.5:p.Asp146Ala
ENST00000524810.5:c.369A>C
ENST00000525419.5:c.383A>C	ENSP00000433521.1:p.Asp128Ala
ENST00000526339.5:c.437A>C	ENSP00000436287.1:p.Asp146Ala
ENST00000526446.5:c.*492A>C	ENSP00000433645.1:n.*492A>C
ENST00000528492.1:c.-2A>C	ENSP00000432848.1:n.-2A>C
ENST00000531282.1:n.289A>C
NM_002496.3:c.437A>C	NP_002487.1:p.Asp146Ala
XM_005274013.1:c.437A>C	XP_005274070.1:p.Asp146Ala
XM_005274014.1:c.437A>C	XP_005274071.1:p.Asp146Ala
XM_005274015.1:c.317A>C	XP_005274072.1:p.Asp106Ala
XM_011545053.1:c.437A>C	XP_011543355.1:p.Asp146Ala
NM_002496.4:c.437A>C MANE Select	NP_002487.1:p.Asp146Ala