Canonical Allele Identifier: CA2634920781

Gene: ACSF3

Linked Data

• dbSNP Id: rs2151564935
• gnomAD v4: 16-89146050-GTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89146051_89146052del , CM000678.2:g.89146051_89146052del	GRCh38
NC_000016.9:g.89212459_89212460del , CM000678.1:g.89212459_89212460del	GRCh37
NC_000016.8:g.87739960_87739961del	NCBI36
NG_031961.1:g.57243_57244del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1613+2_1613+3del	ENSP00000320646.4:n.1613+2_1613+3del
ENST00000614302.5:c.1613+2_1613+3del MANE Select	ENSP00000479130.1:n.1613+2_1613+3del
ENST00000649953.1:c.1823+2_1823+3del	ENSP00000497456.1:n.1823+2_1823+3del
ENST00000317447.8:c.1613+2_1613+3del	ENSP00000320646.4:n.1613+2_1613+3del
ENST00000378345.8:c.818+2_818+3del	ENSP00000367596.4:n.818+2_818+3del
ENST00000406948.7:c.1613+2_1613+3del	ENSP00000384627.3:n.1613+2_1613+3del
ENST00000535176.1:c.100+2_100+3del
ENST00000537116.5:n.739+2_739+3del
ENST00000537155.1:n.353+2_353+3del
ENST00000542688.5:c.*357+2_*357+3del	ENSP00000446281.1:n.*357+2_*357+3del
ENST00000614302.4:c.1613+2_1613+3del	ENSP00000479130.1:n.1613+2_1613+3del
NM_001127214.3:c.1613+2_1613+3del	NP_001120686.1:n.1613+2_1613+3del
NM_001243279.2:c.1613+2_1613+3del	NP_001230208.1:n.1613+2_1613+3del
NM_001284316.1:c.818+2_818+3del	NP_001271245.1:n.818+2_818+3del
NM_174917.4:c.1613+2_1613+3del	NP_777577.2:n.1613+2_1613+3del
NR_045667.2:n.739+2_739+3del
NR_104293.1:n.2047+2_2047+3del
XM_005256293.1:c.1613+2_1613+3del	XP_005256350.1:n.1613+2_1613+3del
XM_011522942.1:c.1613+2_1613+3del	XP_011521244.1:n.1613+2_1613+3del
XM_011522943.1:c.1613+2_1613+3del	XP_011521245.1:n.1613+2_1613+3del
XR_933239.1:n.2054+2_2054+3del
XR_933240.1:n.2051+2_2051+3del
XR_933241.1:n.1808+2_1808+3del
NR_147928.1:n.2091+2_2091+3del
NR_147929.1:n.1845+2_1845+3del
XM_005256293.2:c.1613+2_1613+3del	XP_005256350.1:n.1613+2_1613+3del
XM_017023018.1:c.1613+2_1613+3del	XP_016878507.1:n.1613+2_1613+3del
XM_017023019.1:c.1613+2_1613+3del	XP_016878508.1:n.1613+2_1613+3del
XM_017023020.2:c.-3492+2_-3492+3del	XP_016878509.1:n.-3492+2_-3492+3del
XM_017023022.1:c.746+2_746+3del	XP_016878511.1:n.746+2_746+3del
XM_024450186.1:c.818+2_818+3del	XP_024305954.1:n.818+2_818+3del
XM_024450187.1:c.818+2_818+3del	XP_024305955.1:n.818+2_818+3del
XR_001751864.2:n.1860+2_1860+3del
XR_001751865.1:n.1807+2_1807+3del
XR_933240.3:n.2050+2_2050+3del
NM_001127214.4:c.1613+2_1613+3del	NP_001120686.1:n.1613+2_1613+3del
NM_001243279.3:c.1613+2_1613+3del MANE Select	NP_001230208.1:n.1613+2_1613+3del
NM_001284316.2:c.818+2_818+3del	NP_001271245.1:n.818+2_818+3del
NM_174917.5:c.1613+2_1613+3del	NP_777577.2:n.1613+2_1613+3del
NR_104293.2:n.2004+2_2004+3del
NR_147928.2:n.2048+2_2048+3del
NR_147929.2:n.1802+2_1802+3del