Canonical Allele Identifier: CA338084676

Gene: ACOT7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6385534T>C , CM000663.2:g.6385534T>C	GRCh38
NC_000001.10:g.6445594T>C , CM000663.1:g.6445594T>C	GRCh37
NC_000001.9:g.6368181T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361521.9:c.143+7723A>G MANE Select	ENSP00000354615.4:n.143+7723A>G
ENST00000361521.8:c.143+7723A>G	ENSP00000354615.4:n.143+7723A>G
ENST00000377855.6:c.133A>G	ENSP00000367086.2:p.Arg45Gly
ENST00000377860.8:c.47+7723A>G	ENSP00000367091.4:n.47+7723A>G
ENST00000418124.5:c.47+7723A>G	ENSP00000402532.1:n.47+7723A>G
ENST00000545482.5:c.143+7723A>G	ENSP00000439218.2:n.143+7723A>G
ENST00000608083.5:c.47+7723A>G	ENSP00000476610.1:n.47+7723A>G
NM_007274.3:c.143+7723A>G	NP_009205.3:n.143+7723A>G
NM_181864.2:c.133A>G	NP_863654.1:p.Arg45Gly
NM_181864.3:c.133A>G	NP_863654.1:p.Arg45Gly
NM_007274.4:c.143+7723A>G MANE Select	NP_009205.3:n.143+7723A>G