Canonical Allele Identifier: CA216219

Gene: ACLY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41909581G>T , CM000679.2:g.41909581G>T	GRCh38
NC_000017.10:g.40065834G>T , CM000679.1:g.40065834G>T	GRCh37
NC_000017.9:g.37319360G>T	NCBI36
NG_047031.1:g.25962C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001096.3:c.465C>A MANE Select	NP_001087.2:p.Gly155=
ENST00000352035.7:c.465C>A MANE Select	ENSP00000253792.2:p.Gly155=
NM_001096.2:c.465C>A	NP_001087.2:p.Gly155=
NM_001303274.1:c.627C>A	NP_001290203.1:p.Gly209=
NM_001303275.1:c.627C>A	NP_001290204.1:p.Gly209=
NM_198830.1:c.465C>A	NP_942127.1:p.Gly155=
NM_198830.2:c.465C>A	NP_942127.1:p.Gly155=
ENST00000352035.6:c.465C>A	ENSP00000253792.2:p.Gly155=
ENST00000353196.5:c.465C>A	ENSP00000345398.1:p.Gly155=
ENST00000393896.6:c.465C>A	ENSP00000377474.1:p.Gly155=
ENST00000537919.5:c.282+2839C>A	ENSP00000445349.1:n.282+2839C>A
ENST00000590151.5:c.465C>A	ENSP00000466259.1:p.Gly155=
ENST00000590735.1:n.255C>A
ENST00000590770.5:c.-112-3923C>A	ENSP00000464717.1:n.-112-3923C>A
XM_005257395.1:c.465C>A	XP_005257452.1:p.Gly155=
XM_017024688.1:c.465C>A	XP_016880177.1:p.Gly155=