Canonical Allele Identifier: CA397139201
Community Standard Title: NM_001243279.3(ACSF3):c.880C>T (p.Pro294Ser)
Gene: ACSF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89112149C>T , CM000678.2:g.89112149C>T GRCh38
NC_000016.9:g.89178557C>T , CM000678.1:g.89178557C>T GRCh37
NC_000016.8:g.87706058C>T NCBI36
NG_031961.1:g.23341C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001243279.3:c.880C>T MANE Select NP_001230208.1:p.Pro294Ser
ENST00000614302.5:c.880C>T MANE Select ENSP00000479130.1:p.Pro294Ser
NM_001127214.3:c.880C>T NP_001120686.1:p.Pro294Ser
NM_001127214.4:c.880C>T NP_001120686.1:p.Pro294Ser
NM_001243279.2:c.880C>T NP_001230208.1:p.Pro294Ser
NM_001284316.1:c.85C>T NP_001271245.1:p.Pro29Ser
NM_001284316.2:c.85C>T NP_001271245.1:p.Pro29Ser
NM_174917.4:c.880C>T NP_777577.2:p.Pro294Ser
NM_174917.5:c.880C>T NP_777577.2:p.Pro294Ser
NR_104293.1:n.1261C>T
NR_104293.2:n.1218C>T
NR_147928.1:n.1261C>T
NR_147928.2:n.1218C>T
NR_147929.1:n.1261C>T
NR_147929.2:n.1218C>T
ENST00000317447.8:c.880C>T ENSP00000320646.4:p.Pro294Ser
ENST00000317447.9:c.880C>T ENSP00000320646.4:p.Pro294Ser
ENST00000378345.8:c.85C>T ENSP00000367596.4:p.Pro29Ser
ENST00000406948.7:c.880C>T ENSP00000384627.3:p.Pro294Ser
ENST00000537895.5:c.85C>T ENSP00000439201.1:p.Pro29Ser
ENST00000538340.5:c.205C>T ENSP00000445870.1:p.Pro69Ser
ENST00000540697.5:c.85C>T ENSP00000445397.1:p.Pro29Ser
ENST00000542688.5:c.880C>T ENSP00000446281.1:p.Pro294Ser
ENST00000543676.1:c.122C>T
ENST00000544543.5:c.85C>T ENSP00000442781.1:p.Pro29Ser
ENST00000614302.4:c.880C>T ENSP00000479130.1:p.Pro294Ser
ENST00000649953.1:c.880C>T ENSP00000497456.1:p.Pro294Ser
XM_005256293.1:c.880C>T XP_005256350.1:p.Pro294Ser
XM_005256293.2:c.880C>T XP_005256350.1:p.Pro294Ser
XM_011522942.1:c.880C>T XP_011521244.1:p.Pro294Ser
XM_011522943.1:c.880C>T XP_011521245.1:p.Pro294Ser
XM_011522944.1:c.880C>T XP_011521246.1:p.Pro294Ser
XM_017023018.1:c.880C>T XP_016878507.1:p.Pro294Ser
XM_017023019.1:c.880C>T XP_016878508.1:p.Pro294Ser
XM_017023020.2:c.-4129C>T XP_016878509.1:n.-4129C>T
XM_017023021.1:c.880C>T XP_016878510.1:p.Pro294Ser
XM_024450186.1:c.85C>T XP_024305954.1:p.Pro29Ser
XM_024450187.1:c.85C>T XP_024305955.1:p.Pro29Ser
XR_001751864.2:n.1223C>T
XR_001751865.1:n.1223C>T
XR_933238.1:n.1224C>T
XR_933238.2:n.1223C>T
XR_933239.1:n.1224C>T
XR_933240.1:n.1224C>T
XR_933240.3:n.1223C>T
XR_933241.1:n.1224C>T