Canonical Allele Identifier: CA390372421

Gene: FAM161B COQ6

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.73950129G>C , CM000676.2:g.73950129G>C	GRCh38
NC_000014.8:g.74416832G>C , CM000676.1:g.74416832G>C	GRCh37
NC_000014.7:g.73486585G>C	NCBI36
NG_032805.1:g.5196G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651776.1:c.87C>G (FAM161B)	ENSP00000499021.1:p.Asp29Glu
ENST00000286544.3:c.87C>G (FAM161B)	ENSP00000286544.3:p.Asp29Glu
ENST00000394026.8:c.37G>C (COQ6)	ENSP00000377594.4:p.Val13Leu
ENST00000554341.6:c.37G>C (COQ6)	ENSP00000450736.2:p.Val13Leu
NM_152445.2:c.87C>G (FAM161B)	NP_689658.2:p.Asp29Glu
NM_182480.2:c.37G>C (COQ6)	NP_872286.2:p.Val13Leu
XM_011536475.1:c.87C>G (FAM161B)	XP_011534777.1:p.Asp29Glu
XM_011536809.1:c.-55G>C (COQ6)	XP_011535111.1:n.-55G>C
XM_011536475.2:c.87C>G (FAM161B)	XP_011534777.1:p.Asp29Glu
XM_011536809.3:c.-55G>C (COQ6)	XP_011535111.1:n.-55G>C
NM_182480.3:c.37G>C (COQ6)	NP_872286.2:p.Val13Leu