Canonical Allele Identifier: CA2634920458
Gene: ACSF3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89145269dup , CM000678.2:g.89145269dup GRCh38
NC_000016.9:g.89211677dup , CM000678.1:g.89211677dup GRCh37
NC_000016.8:g.87739178dup NCBI36
NG_031961.1:g.56461dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000317447.9:c.1369dup
ENST00000614302.5:c.1369dup
ENST00000649953.1:c.1579dup
ENST00000317447.8:c.1369dup
ENST00000378345.8:c.574dup
ENST00000406948.7:c.1369dup
ENST00000537116.5:n.495dup
ENST00000537155.1:n.109dup
ENST00000542688.5:c.*113dup
ENST00000544543.5:c.574dup
ENST00000562204.1:n.342dup
ENST00000614302.4:c.1369dup
NM_001127214.3:c.1369dup
NM_001243279.2:c.1369dup
NM_001284316.1:c.574dup
NM_174917.4:c.1369dup
NR_045667.2:n.495dup
NR_104293.1:n.1803dup
XM_005256293.1:c.1369dup
XM_011522942.1:c.1369dup
XM_011522943.1:c.1369dup
XR_933239.1:n.1810dup
XR_933240.1:n.1807dup
XR_933241.1:n.1564dup
NR_147928.1:n.1847dup
NR_147929.1:n.1601dup
XM_005256293.2:c.1369dup
XM_017023018.1:c.1369dup
XM_017023019.1:c.1369dup
XM_017023020.2:c.-3736dup XP_016878509.1:n.-3736dup
XM_017023022.1:c.502dup
XM_024450186.1:c.574dup
XM_024450187.1:c.574dup
XR_001751864.2:n.1616dup
XR_001751865.1:n.1563dup
XR_933240.3:n.1806dup
NM_001127214.4:c.1369dup
NM_001243279.3:c.1369dup
NM_001284316.2:c.574dup
NM_174917.5:c.1369dup
NR_104293.2:n.1760dup
NR_147928.2:n.1804dup
NR_147929.2:n.1558dup