Canonical Allele Identifier: CA980387272
Gene: ACSF3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89101173_89101174insTTTTTTCAT , CM000678.2:g.89101173_89101174insTTTTTTCAT GRCh38
NC_000016.9:g.89167581_89167582insTTTTTTCAT , CM000678.1:g.89167581_89167582insTTTTTTCAT GRCh37
NC_000016.8:g.87695082_87695083insTTTTTTCAT NCBI36
NG_031961.1:g.12365_12366insTTTTTTCAT

Transcript Alleles

HGVS Amino-acid change
ENST00000317447.9:c.492_493insTTTTTTCAT ENSP00000320646.4:p.Gly164_Val165insPhePh...
ENST00000614302.5:c.492_493insTTTTTTCAT MANE Select ENSP00000479130.1:p.Gly164_Val165insPhePh...
ENST00000649953.1:c.492_493insTTTTTTCAT ENSP00000497456.1:p.Gly164_Val165insPhePh...
ENST00000317447.8:c.492_493insTTTTTTCAT ENSP00000320646.4:p.Gly164_Val165insPhePh...
ENST00000378345.8:c.-129-1431_-129-1430insTTTTTTCAT ENSP00000367596.4:n.-129-1431_-129-1430in...
ENST00000406948.7:c.492_493insTTTTTTCAT ENSP00000384627.3:p.Gly164_Val165insPhePh...
ENST00000537290.5:c.492_493insTTTTTTCAT ENSP00000440734.1:p.Gly164_Val165insPhePh...
ENST00000537895.5:c.-129-1431_-129-1430insTTTTTTCAT ENSP00000439201.1:n.-129-1431_-129-1430in...
ENST00000540697.5:c.-129-1431_-129-1430insTTTTTTCAT ENSP00000445397.1:n.-129-1431_-129-1430in...
ENST00000542688.5:c.492_493insTTTTTTCAT ENSP00000446281.1:p.Gly164_Val165insPhePh...
ENST00000614302.4:c.492_493insTTTTTTCAT ENSP00000479130.1:p.Gly164_Val165insPhePh...
NM_001127214.3:c.492_493insTTTTTTCAT NP_001120686.1:p.Gly164_Val165insPhePheHi...
NM_001243279.2:c.492_493insTTTTTTCAT NP_001230208.1:p.Gly164_Val165insPhePheHi...
NM_001284316.1:c.-129-1431_-129-1430insTTTTTTCAT NP_001271245.1:n.-129-1431_-129-1430insTT...
NM_174917.4:c.492_493insTTTTTTCAT NP_777577.2:p.Gly164_Val165insPhePheHis
NR_104293.1:n.873_874insTTTTTTCAT
XM_005256293.1:c.492_493insTTTTTTCAT XP_005256350.1:p.Gly164_Val165insPhePheHi...
XM_011522942.1:c.492_493insTTTTTTCAT XP_011521244.1:p.Gly164_Val165insPhePheHi...
XM_011522943.1:c.492_493insTTTTTTCAT XP_011521245.1:p.Gly164_Val165insPhePheHi...
XM_011522944.1:c.492_493insTTTTTTCAT XP_011521246.1:p.Gly164_Val165insPhePheHi...
XR_933238.1:n.836_837insTTTTTTCAT
XR_933239.1:n.836_837insTTTTTTCAT
XR_933240.1:n.836_837insTTTTTTCAT
XR_933241.1:n.836_837insTTTTTTCAT
NR_147928.1:n.873_874insTTTTTTCAT
NR_147929.1:n.873_874insTTTTTTCAT
XM_005256293.2:c.492_493insTTTTTTCAT XP_005256350.1:p.Gly164_Val165insPhePheHi...
XM_017023018.1:c.492_493insTTTTTTCAT XP_016878507.1:p.Gly164_Val165insPhePheHi...
XM_017023019.1:c.492_493insTTTTTTCAT XP_016878508.1:p.Gly164_Val165insPhePheHi...
XM_017023020.2:c.-4517_-4516insTTTTTTCAT XP_016878509.1:n.-4517_-4516insTTTTTTCAT
XM_017023021.1:c.492_493insTTTTTTCAT XP_016878510.1:p.Gly164_Val165insPhePheHi...
XM_024450186.1:c.-129-1431_-129-1430insTTTTTTCAT XP_024305954.1:n.-129-1431_-129-1430insTT...
XM_024450187.1:c.-129-1431_-129-1430insTTTTTTCAT XP_024305955.1:n.-129-1431_-129-1430insTT...
XR_001751864.2:n.835_836insTTTTTTCAT
XR_001751865.1:n.835_836insTTTTTTCAT
XR_933238.2:n.835_836insTTTTTTCAT
XR_933240.3:n.835_836insTTTTTTCAT
NM_001127214.4:c.492_493insTTTTTTCAT NP_001120686.1:p.Gly164_Val165insPhePheHi...
NM_001243279.3:c.492_493insTTTTTTCAT MANE Select NP_001230208.1:p.Gly164_Val165insPhePheHi...
NM_001284316.2:c.-129-1431_-129-1430insTTTTTTCAT NP_001271245.1:n.-129-1431_-129-1430insTT...
NM_174917.5:c.492_493insTTTTTTCAT NP_777577.2:p.Gly164_Val165insPhePheHis
NR_104293.2:n.830_831insTTTTTTCAT
NR_147928.2:n.830_831insTTTTTTCAT
NR_147929.2:n.830_831insTTTTTTCAT