Canonical Allele Identifier: CA397139403
Community Standard Title: NM_001243279.3(ACSF3):c.940C>T (p.Gln314Ter)
Gene: ACSF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89112209C>T , CM000678.2:g.89112209C>T GRCh38
NC_000016.9:g.89178617C>T , CM000678.1:g.89178617C>T GRCh37
NC_000016.8:g.87706118C>T NCBI36
NG_031961.1:g.23401C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001243279.3:c.940C>T MANE Select NP_001230208.1:p.Gln314Ter
ENST00000614302.5:c.940C>T MANE Select ENSP00000479130.1:p.Gln314Ter
NM_001127214.3:c.940C>T NP_001120686.1:p.Gln314Ter
NM_001127214.4:c.940C>T NP_001120686.1:p.Gln314Ter
NM_001243279.2:c.940C>T NP_001230208.1:p.Gln314Ter
NM_001284316.1:c.145C>T NP_001271245.1:p.Gln49Ter
NM_001284316.2:c.145C>T NP_001271245.1:p.Gln49Ter
NM_174917.4:c.940C>T NP_777577.2:p.Gln314Ter
NM_174917.5:c.940C>T NP_777577.2:p.Gln314Ter
NR_104293.1:n.1321C>T
NR_104293.2:n.1278C>T
NR_147928.1:n.1321C>T
NR_147928.2:n.1278C>T
NR_147929.1:n.1321C>T
NR_147929.2:n.1278C>T
ENST00000317447.8:c.940C>T ENSP00000320646.4:p.Gln314Ter
ENST00000317447.9:c.940C>T ENSP00000320646.4:p.Gln314Ter
ENST00000378345.8:c.145C>T ENSP00000367596.4:p.Gln49Ter
ENST00000406948.7:c.940C>T ENSP00000384627.3:p.Gln314Ter
ENST00000537895.5:c.145C>T ENSP00000439201.1:p.Gln49Ter
ENST00000538340.5:c.265C>T ENSP00000445870.1:p.Gln89Ter
ENST00000540697.5:c.145C>T ENSP00000445397.1:p.Gln49Ter
ENST00000542688.5:c.940C>T ENSP00000446281.1:p.Gln314Ter
ENST00000543676.1:c.182C>T
ENST00000544543.5:c.145C>T ENSP00000442781.1:p.Gln49Ter
ENST00000562204.1:n.9C>T
ENST00000614302.4:c.940C>T ENSP00000479130.1:p.Gln314Ter
ENST00000649953.1:c.940C>T ENSP00000497456.1:p.Gln314Ter
XM_005256293.1:c.940C>T XP_005256350.1:p.Gln314Ter
XM_005256293.2:c.940C>T XP_005256350.1:p.Gln314Ter
XM_011522942.1:c.940C>T XP_011521244.1:p.Gln314Ter
XM_011522943.1:c.940C>T XP_011521245.1:p.Gln314Ter
XM_011522944.1:c.940C>T XP_011521246.1:p.Gln314Ter
XM_017023018.1:c.940C>T XP_016878507.1:p.Gln314Ter
XM_017023019.1:c.940C>T XP_016878508.1:p.Gln314Ter
XM_017023020.2:c.-4069C>T XP_016878509.1:n.-4069C>T
XM_017023021.1:c.940C>T XP_016878510.1:p.Gln314Ter
XM_024450186.1:c.145C>T XP_024305954.1:p.Gln49Ter
XM_024450187.1:c.145C>T XP_024305955.1:p.Gln49Ter
XR_001751864.2:n.1283C>T
XR_001751865.1:n.1283C>T
XR_933238.1:n.1284C>T
XR_933238.2:n.1283C>T
XR_933239.1:n.1284C>T
XR_933240.1:n.1284C>T
XR_933240.3:n.1283C>T
XR_933241.1:n.1284C>T