Canonical Allele Identifier: CA497146299
Gene: ACSF3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.89211805C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89145397C>T , CM000678.2:g.89145397C>T GRCh38
NC_000016.9:g.89211805C>T , CM000678.1:g.89211805C>T GRCh37
NC_000016.8:g.87739306C>T NCBI36
NG_031961.1:g.56589C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000317447.9:c.1497C>T ENSP00000320646.4:p.Ile499=
ENST00000614302.5:c.1497C>T MANE Select ENSP00000479130.1:p.Ile499=
ENST00000649953.1:c.1707C>T ENSP00000497456.1:p.Ile569=
ENST00000317447.8:c.1497C>T ENSP00000320646.4:p.Ile499=
ENST00000378345.8:c.702C>T ENSP00000367596.4:p.Ile234=
ENST00000406948.7:c.1497C>T ENSP00000384627.3:p.Ile499=
ENST00000537116.5:n.623C>T
ENST00000537155.1:n.237C>T
ENST00000542688.5:c.*241C>T ENSP00000446281.1:n.*241C>T
ENST00000544543.5:c.702C>T ENSP00000442781.1:p.Ile234=
ENST00000562204.1:n.470C>T
ENST00000614302.4:c.1497C>T ENSP00000479130.1:p.Ile499=
NM_001127214.3:c.1497C>T NP_001120686.1:p.Ile499=
NM_001243279.2:c.1497C>T NP_001230208.1:p.Ile499=
NM_001284316.1:c.702C>T NP_001271245.1:p.Ile234=
NM_174917.4:c.1497C>T NP_777577.2:p.Ile499=
NR_045667.2:n.623C>T
NR_104293.1:n.1931C>T
XM_005256293.1:c.1497C>T XP_005256350.1:p.Ile499=
XM_011522942.1:c.1497C>T XP_011521244.1:p.Ile499=
XM_011522943.1:c.1497C>T XP_011521245.1:p.Ile499=
XR_933239.1:n.1938C>T
XR_933240.1:n.1935C>T
XR_933241.1:n.1692C>T
NR_147928.1:n.1975C>T
NR_147929.1:n.1729C>T
XM_005256293.2:c.1497C>T XP_005256350.1:p.Ile499=
XM_017023018.1:c.1497C>T XP_016878507.1:p.Ile499=
XM_017023019.1:c.1497C>T XP_016878508.1:p.Ile499=
XM_017023020.2:c.-3608C>T XP_016878509.1:n.-3608C>T
XM_017023022.1:c.630C>T XP_016878511.1:p.Ile210=
XM_024450186.1:c.702C>T XP_024305954.1:p.Ile234=
XM_024450187.1:c.702C>T XP_024305955.1:p.Ile234=
XR_001751864.2:n.1744C>T
XR_001751865.1:n.1691C>T
XR_933240.3:n.1934C>T
NM_001127214.4:c.1497C>T NP_001120686.1:p.Ile499=
NM_001243279.3:c.1497C>T MANE Select NP_001230208.1:p.Ile499=
NM_001284316.2:c.702C>T NP_001271245.1:p.Ile234=
NM_174917.5:c.1497C>T NP_777577.2:p.Ile499=
NR_104293.2:n.1888C>T
NR_147928.2:n.1932C>T
NR_147929.2:n.1686C>T