Canonical Allele Identifier: CA1140186317

Gene: ACOT7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6283765G= , CM000663.2:g.6283765G=	GRCh38
NC_000001.10:g.6343825G= , CM000663.1:g.6343825G=	GRCh37
NC_000001.9:g.6266412G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361521.9:c.830-2479C= MANE Select	ENSP00000354615.4:n.830-2479C=
ENST00000361521.8:c.830-2479C=	ENSP00000354615.4:n.830-2479C=
ENST00000377842.7:c.707-2479C=	ENSP00000367073.3:n.707-2479C=
ENST00000377845.7:c.770-2479C=	ENSP00000367076.3:n.770-2479C=
ENST00000377855.6:c.860-2479C=	ENSP00000367086.2:n.860-2479C=
ENST00000377860.8:c.734-969C=	ENSP00000367091.4:n.734-969C=
ENST00000418124.5:c.734-877C=	ENSP00000402532.1:n.734-877C=
ENST00000473466.2:c.683-2479C=	ENSP00000465719.1:n.683-2479C=
ENST00000481175.1:n.642-969C=
ENST00000545482.5:c.830-2479C=	ENSP00000439218.2:n.830-2479C=
ENST00000608083.5:c.734-2479C=	ENSP00000476610.1:n.734-2479C=
NM_007274.3:c.830-2479C=	NP_009205.3:n.830-2479C=
NM_181864.2:c.860-2479C=	NP_863654.1:n.860-2479C=
NM_181865.2:c.770-2479C=	NP_863655.1:n.770-2479C=
NM_181866.2:c.707-2479C=	NP_863656.1:n.707-2479C=
NM_181864.3:c.860-2479C=	NP_863654.1:n.860-2479C=
NM_181865.3:c.770-2479C=	NP_863655.1:n.770-2479C=
NM_181866.3:c.707-2479C=	NP_863656.1:n.707-2479C=
NM_007274.4:c.830-2479C= MANE Select	NP_009205.3:n.830-2479C=