Canonical Allele Identifier: CA15734868

Gene: ACSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.81150757C>T , CM000674.2:g.81150757C>T	GRCh38
NC_000012.11:g.81544536C>T , CM000674.1:g.81544536C>T	GRCh37
NC_000012.10:g.80068667C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_024560.4:c.922-1087C>T MANE Select	NP_078836.1:n.922-1087C>T
ENST00000548058.6:c.922-1087C>T MANE Select	ENSP00000449535.1:n.922-1087C>T
NM_001330242.1:c.919-1087C>T	NP_001317171.1:n.919-1087C>T
NM_001330242.2:c.919-1087C>T	NP_001317171.1:n.919-1087C>T
NM_001330243.1:c.-33-1087C>T	NP_001317172.1:n.-33-1087C>T
NM_001330243.2:c.-33-1087C>T	NP_001317172.1:n.-33-1087C>T
NM_024560.2:c.922-1087C>T	NP_078836.1:n.922-1087C>T
NM_024560.3:c.922-1087C>T	NP_078836.1:n.922-1087C>T
ENST00000261206.7:c.919-1087C>T	ENSP00000261206.3:n.919-1087C>T
ENST00000548058.5:c.922-1087C>T	ENSP00000449535.1:n.922-1087C>T
XM_005269150.2:c.919-1087C>T	XP_005269207.1:n.919-1087C>T
XM_005269151.3:c.922-1087C>T	XP_005269208.1:n.922-1087C>T
XM_005269151.5:c.922-1087C>T	XP_005269208.1:n.922-1087C>T
XM_011538740.1:c.-33-1087C>T	XP_011537042.1:n.-33-1087C>T
XR_944720.1:n.1025-1087C>T
XR_944720.3:n.1006-1087C>T