Canonical Allele Identifier: CA2695201153
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2680483
ClinVar RCV Id: RCV003474512

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89145226_89145298delinsATCCG , CM000678.2:g.89145226_89145298delinsATCCG GRCh38
NC_000016.9:g.89211634_89211706delinsATCCG , CM000678.1:g.89211634_89211706delinsATCCG GRCh37
NC_000016.8:g.87739135_87739207delinsATCCG NCBI36
NG_031961.1:g.56418_56490delinsATCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000317447.9:c.1367-41_1398delinsATCCG
ENST00000614302.5:c.1367-41_1398delinsATCCG
ENST00000649953.1:c.1577-41_1608delinsATCCG
ENST00000317447.8:c.1367-41_1398delinsATCCG
ENST00000378345.8:c.572-41_603delinsATCCG
ENST00000406948.7:c.1367-41_1398delinsATCCG
ENST00000537116.5:n.493-41_524delinsATCCG
ENST00000537155.1:n.66_138delinsATCCG
ENST00000542688.5:c.*111-41_*142delinsATCCG
ENST00000544543.5:c.572-41_603delinsATCCG
ENST00000562204.1:n.299_371delinsATCCG
ENST00000614302.4:c.1367-41_1398delinsATCCG
NM_001127214.3:c.1367-41_1398delinsATCCG
NM_001243279.2:c.1367-41_1398delinsATCCG
NM_001284316.1:c.572-41_603delinsATCCG
NM_174917.4:c.1367-41_1398delinsATCCG
NR_045667.2:n.493-41_524delinsATCCG
NR_104293.1:n.1760_1832delinsATCCG
XM_005256293.1:c.1367-41_1398delinsATCCG
XM_011522942.1:c.1367-41_1398delinsATCCG
XM_011522943.1:c.1367-41_1398delinsATCCG
XR_933239.1:n.1808-41_1839delinsATCCG
XR_933240.1:n.1805-41_1836delinsATCCG
XR_933241.1:n.1562-41_1593delinsATCCG
NR_147928.1:n.1845-41_1876delinsATCCG
NR_147929.1:n.1599-41_1630delinsATCCG
XM_005256293.2:c.1367-41_1398delinsATCCG
XM_017023018.1:c.1367-41_1398delinsATCCG
XM_017023019.1:c.1367-41_1398delinsATCCG
XM_017023020.2:c.-3779_-3707delinsATCCG XP_016878509.1:n.-3779_-3707delinsATCCG
XM_017023022.1:c.500-41_531delinsATCCG
XM_024450186.1:c.572-41_603delinsATCCG
XM_024450187.1:c.572-41_603delinsATCCG
XR_001751864.2:n.1573_1645delinsATCCG
XR_001751865.1:n.1561-41_1592delinsATCCG
XR_933240.3:n.1804-41_1835delinsATCCG
NM_001127214.4:c.1367-41_1398delinsATCCG
NM_001243279.3:c.1367-41_1398delinsATCCG
NM_001284316.2:c.572-41_603delinsATCCG
NM_174917.5:c.1367-41_1398delinsATCCG
NR_104293.2:n.1717_1789delinsATCCG
NR_147928.2:n.1802-41_1833delinsATCCG
NR_147929.2:n.1556-41_1587delinsATCCG