Canonical Allele Identifier: CA2356677126

Gene: ACSS1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.25038463G= , CM000682.2:g.25038463G=	GRCh38
NC_000020.10:g.25019099G= , CM000682.1:g.25019099G=	GRCh37
NC_000020.9:g.24967099G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032501.4:c.432-7505C= MANE Select	NP_115890.2:n.432-7505C=
ENST00000323482.9:c.432-7505C= MANE Select	ENSP00000316924.4:n.432-7505C=
NM_001252675.1:c.432-7505C=	NP_001239604.1:n.432-7505C=
NM_001252675.2:c.432-7505C=	NP_001239604.1:n.432-7505C=
NM_001252677.1:c.432-7505C=	NP_001239606.1:n.432-7505C=
NM_001252677.2:c.432-7505C=	NP_001239606.1:n.432-7505C=
NM_032501.3:c.432-7505C=	NP_115890.2:n.432-7505C=
ENST00000323482.8:c.432-7505C=	ENSP00000316924.4:n.432-7505C=
ENST00000432802.6:c.432-7505C=	ENSP00000388793.2:n.432-7505C=
XM_006723659.1:c.432-7505C=	XP_006723722.1:n.432-7505C=
XM_011529388.1:c.-47-7505C=	XP_011527690.1:n.-47-7505C=
XR_937170.1:n.473-7505C=