Canonical Allele Identifier: CA397138099

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89102757C>T , CM000678.2:g.89102757C>T	GRCh38
NC_000016.9:g.89169165C>T , CM000678.1:g.89169165C>T	GRCh37
NC_000016.8:g.87696666C>T	NCBI36
NG_031961.1:g.13949C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001243279.3:c.820C>T MANE Select	NP_001230208.1:p.Gln274Ter
ENST00000614302.5:c.820C>T MANE Select	ENSP00000479130.1:p.Gln274Ter
NM_001127214.3:c.820C>T	NP_001120686.1:p.Gln274Ter
NM_001127214.4:c.820C>T	NP_001120686.1:p.Gln274Ter
NM_001243279.2:c.820C>T	NP_001230208.1:p.Gln274Ter
NM_001284316.1:c.25C>T	NP_001271245.1:p.Gln9Ter
NM_001284316.2:c.25C>T	NP_001271245.1:p.Gln9Ter
NM_174917.4:c.820C>T	NP_777577.2:p.Gln274Ter
NM_174917.5:c.820C>T	NP_777577.2:p.Gln274Ter
NR_104293.1:n.1201C>T
NR_104293.2:n.1158C>T
NR_147928.1:n.1201C>T
NR_147928.2:n.1158C>T
NR_147929.1:n.1201C>T
NR_147929.2:n.1158C>T
ENST00000317447.8:c.820C>T	ENSP00000320646.4:p.Gln274Ter
ENST00000317447.9:c.820C>T	ENSP00000320646.4:p.Gln274Ter
ENST00000378345.8:c.25C>T	ENSP00000367596.4:p.Gln9Ter
ENST00000406948.7:c.820C>T	ENSP00000384627.3:p.Gln274Ter
ENST00000537895.5:c.25C>T	ENSP00000439201.1:p.Gln9Ter
ENST00000538340.5:c.145C>T	ENSP00000445870.1:p.Gln49Ter
ENST00000540697.5:c.25C>T	ENSP00000445397.1:p.Gln9Ter
ENST00000542688.5:c.820C>T	ENSP00000446281.1:p.Gln274Ter
ENST00000543676.1:c.62C>T
ENST00000544543.5:c.25C>T	ENSP00000442781.1:p.Gln9Ter
ENST00000614302.4:c.820C>T	ENSP00000479130.1:p.Gln274Ter
ENST00000649953.1:c.820C>T	ENSP00000497456.1:p.Gln274Ter
XM_005256293.1:c.820C>T	XP_005256350.1:p.Gln274Ter
XM_005256293.2:c.820C>T	XP_005256350.1:p.Gln274Ter
XM_011522942.1:c.820C>T	XP_011521244.1:p.Gln274Ter
XM_011522943.1:c.820C>T	XP_011521245.1:p.Gln274Ter
XM_011522944.1:c.820C>T	XP_011521246.1:p.Gln274Ter
XM_017023018.1:c.820C>T	XP_016878507.1:p.Gln274Ter
XM_017023019.1:c.820C>T	XP_016878508.1:p.Gln274Ter
XM_017023020.2:c.-4189C>T	XP_016878509.1:n.-4189C>T
XM_017023021.1:c.820C>T	XP_016878510.1:p.Gln274Ter
XM_024450186.1:c.25C>T	XP_024305954.1:p.Gln9Ter
XM_024450187.1:c.25C>T	XP_024305955.1:p.Gln9Ter
XR_001751864.2:n.1163C>T
XR_001751865.1:n.1163C>T
XR_933238.1:n.1164C>T
XR_933238.2:n.1163C>T
XR_933239.1:n.1164C>T
XR_933240.1:n.1164C>T
XR_933240.3:n.1163C>T
XR_933241.1:n.1164C>T