Canonical Allele Identifier: CA2634920496

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89145468-AGAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145472_89145474del , CM000678.2:g.89145472_89145474del	GRCh38
NC_000016.9:g.89211880_89211882del , CM000678.1:g.89211880_89211882del	GRCh37
NC_000016.8:g.87739381_87739383del	NCBI36
NG_031961.1:g.56664_56666del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1501+71_1501+73del	ENSP00000320646.4:n.1501+71_1501+73del
ENST00000614302.5:c.1501+71_1501+73del MANE Select	ENSP00000479130.1:n.1501+71_1501+73del
ENST00000649953.1:c.1711+71_1711+73del	ENSP00000497456.1:n.1711+71_1711+73del
ENST00000317447.8:c.1501+71_1501+73del	ENSP00000320646.4:n.1501+71_1501+73del
ENST00000378345.8:c.706+71_706+73del	ENSP00000367596.4:n.706+71_706+73del
ENST00000406948.7:c.1501+71_1501+73del	ENSP00000384627.3:n.1501+71_1501+73del
ENST00000537116.5:n.627+71_627+73del
ENST00000537155.1:n.241+71_241+73del
ENST00000542688.5:c.*245+71_*245+73del	ENSP00000446281.1:n.*245+71_*245+73del
ENST00000562204.1:n.474+71_474+73del
ENST00000614302.4:c.1501+71_1501+73del	ENSP00000479130.1:n.1501+71_1501+73del
NM_001127214.3:c.1501+71_1501+73del	NP_001120686.1:n.1501+71_1501+73del
NM_001243279.2:c.1501+71_1501+73del	NP_001230208.1:n.1501+71_1501+73del
NM_001284316.1:c.706+71_706+73del	NP_001271245.1:n.706+71_706+73del
NM_174917.4:c.1501+71_1501+73del	NP_777577.2:n.1501+71_1501+73del
NR_045667.2:n.627+71_627+73del
NR_104293.1:n.1935+71_1935+73del
XM_005256293.1:c.1501+71_1501+73del	XP_005256350.1:n.1501+71_1501+73del
XM_011522942.1:c.1501+71_1501+73del	XP_011521244.1:n.1501+71_1501+73del
XM_011522943.1:c.1501+71_1501+73del	XP_011521245.1:n.1501+71_1501+73del
XR_933239.1:n.1942+71_1942+73del
XR_933240.1:n.1939+71_1939+73del
XR_933241.1:n.1696+71_1696+73del
NR_147928.1:n.1979+71_1979+73del
NR_147929.1:n.1733+71_1733+73del
XM_005256293.2:c.1501+71_1501+73del	XP_005256350.1:n.1501+71_1501+73del
XM_017023018.1:c.1501+71_1501+73del	XP_016878507.1:n.1501+71_1501+73del
XM_017023019.1:c.1501+71_1501+73del	XP_016878508.1:n.1501+71_1501+73del
XM_017023020.2:c.-3604+71_-3604+73del	XP_016878509.1:n.-3604+71_-3604+73del
XM_017023022.1:c.634+71_634+73del	XP_016878511.1:n.634+71_634+73del
XM_024450186.1:c.706+71_706+73del	XP_024305954.1:n.706+71_706+73del
XM_024450187.1:c.706+71_706+73del	XP_024305955.1:n.706+71_706+73del
XR_001751864.2:n.1748+71_1748+73del
XR_001751865.1:n.1695+71_1695+73del
XR_933240.3:n.1938+71_1938+73del
NM_001127214.4:c.1501+71_1501+73del	NP_001120686.1:n.1501+71_1501+73del
NM_001243279.3:c.1501+71_1501+73del MANE Select	NP_001230208.1:n.1501+71_1501+73del
NM_001284316.2:c.706+71_706+73del	NP_001271245.1:n.706+71_706+73del
NM_174917.5:c.1501+71_1501+73del	NP_777577.2:n.1501+71_1501+73del
NR_104293.2:n.1892+71_1892+73del
NR_147928.2:n.1936+71_1936+73del
NR_147929.2:n.1690+71_1690+73del