Canonical Allele Identifier: CA2241496014
Gene: ACSF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89114446_89114447delinsTG , CM000678.2:g.89114446_89114447delinsTG GRCh38
NC_000016.9:g.89180854_89180855delinsTG , CM000678.1:g.89180854_89180855delinsTG GRCh37
NC_000016.8:g.87708355_87708356delinsTG NCBI36
NG_031961.1:g.25638_25639delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000317447.9:c.1085_1086delinsTG ENSP00000320646.4:p.Met362=
ENST00000614302.5:c.1085_1086delinsTG MANE Select ENSP00000479130.1:p.Met362=
ENST00000649953.1:c.1085_1086delinsTG ENSP00000497456.1:p.Met362=
ENST00000317447.8:c.1085_1086delinsTG ENSP00000320646.4:p.Met362=
ENST00000378345.8:c.290_291delinsTG ENSP00000367596.4:p.Met97=
ENST00000406948.7:c.1085_1086delinsTG ENSP00000384627.3:p.Met362=
ENST00000537895.5:c.290_291delinsTG ENSP00000439201.1:p.Met97=
ENST00000538340.5:c.302+2200_302+2201delinsTG ENSP00000445870.1:n.302+2200_302+2201delinsTG
ENST00000540697.5:c.290_291delinsTG ENSP00000445397.1:p.Met97=
ENST00000542688.5:c.977+2200_977+2201delinsTG ENSP00000446281.1:n.977+2200_977+2201delinsTG
ENST00000543676.1:c.327_328delinsTG
ENST00000544543.5:c.290_291delinsTG ENSP00000442781.1:p.Met97=
ENST00000562204.1:n.46+2200_46+2201delinsTG
ENST00000614302.4:c.1085_1086delinsTG ENSP00000479130.1:p.Met362=
NM_001127214.3:c.1085_1086delinsTG NP_001120686.1:p.Met362=
NM_001243279.2:c.1085_1086delinsTG NP_001230208.1:p.Met362=
NM_001284316.1:c.290_291delinsTG NP_001271245.1:p.Met97=
NM_174917.4:c.1085_1086delinsTG NP_777577.2:p.Met362=
NR_104293.1:n.1466_1467delinsTG
XM_005256293.1:c.1085_1086delinsTG XP_005256350.1:p.Met362=
XM_011522942.1:c.1085_1086delinsTG XP_011521244.1:p.Met362=
XM_011522943.1:c.1085_1086delinsTG XP_011521245.1:p.Met362=
XM_011522944.1:c.1085_1086delinsTG XP_011521246.1:p.Met362=
XR_933238.1:n.1429_1430delinsTG
XR_933239.1:n.1429_1430delinsTG
XR_933240.1:n.1429_1430delinsTG
XR_933241.1:n.1321+2200_1321+2201delinsTG
NR_147928.1:n.1466_1467delinsTG
NR_147929.1:n.1358+2200_1358+2201delinsTG
XM_005256293.2:c.1085_1086delinsTG XP_005256350.1:p.Met362=
XM_017023018.1:c.1085_1086delinsTG XP_016878507.1:p.Met362=
XM_017023019.1:c.1085_1086delinsTG XP_016878508.1:p.Met362=
XM_017023020.2:c.-4032+2200_-4032+2201delinsTG XP_016878509.1:n.-4032+2200_-4032+2201delinsTG
XM_017023021.1:c.1085_1086delinsTG XP_016878510.1:p.Met362=
XM_024450186.1:c.290_291delinsTG XP_024305954.1:p.Met97=
XM_024450187.1:c.290_291delinsTG XP_024305955.1:p.Met97=
XR_001751864.2:n.1320+2200_1320+2201delinsTG
XR_001751865.1:n.1320+2200_1320+2201delinsTG
XR_933238.2:n.1428_1429delinsTG
XR_933240.3:n.1428_1429delinsTG
NM_001127214.4:c.1085_1086delinsTG NP_001120686.1:p.Met362=
NM_001243279.3:c.1085_1086delinsTG MANE Select NP_001230208.1:p.Met362=
NM_001284316.2:c.290_291delinsTG NP_001271245.1:p.Met97=
NM_174917.5:c.1085_1086delinsTG NP_777577.2:p.Met362=
NR_104293.2:n.1423_1424delinsTG
NR_147928.2:n.1423_1424delinsTG
NR_147929.2:n.1315+2200_1315+2201delinsTG