Canonical Allele Identifier: CA2634917664

Gene: ACSF3

Linked Data

• ClinVar Variation Id: 2680447
• ClinVar RCV Id: RCV003460384
• gnomAD v4: 16-89101086-GTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89101088_89101089del , CM000678.2:g.89101088_89101089del	GRCh38
NC_000016.9:g.89167496_89167497del , CM000678.1:g.89167496_89167497del	GRCh37
NC_000016.8:g.87694997_87694998del	NCBI36
NG_031961.1:g.12280_12281del

Transcript Alleles

HGVS	Amino-acid change
ENST00000317447.9:c.407_408del	ENSP00000320646.4:p.Tyr136CysfsTer?
ENST00000614302.5:c.407_408del MANE Select	ENSP00000479130.1:p.Tyr136CysfsTer?
ENST00000649953.1:c.407_408del	ENSP00000497456.1:p.Tyr136CysfsTer?
ENST00000317447.8:c.407_408del	ENSP00000320646.4:p.Tyr136CysfsTer?
ENST00000378345.8:c.-129-1516_-129-1515del	ENSP00000367596.4:n.-129-1516_-129-1515de...
ENST00000406948.7:c.407_408del	ENSP00000384627.3:p.Tyr136CysfsTer?
ENST00000537290.5:c.407_408del	ENSP00000440734.1:p.Tyr136CysfsTer?
ENST00000537895.5:c.-129-1516_-129-1515del	ENSP00000439201.1:n.-129-1516_-129-1515de...
ENST00000540697.5:c.-129-1516_-129-1515del	ENSP00000445397.1:n.-129-1516_-129-1515de...
ENST00000542688.5:c.407_408del	ENSP00000446281.1:p.Tyr136CysfsTer?
ENST00000614302.4:c.407_408del	ENSP00000479130.1:p.Tyr136CysfsTer?
NM_001127214.3:c.407_408del	NP_001120686.1:p.Tyr136CysfsTer?
NM_001243279.2:c.407_408del	NP_001230208.1:p.Tyr136CysfsTer?
NM_001284316.1:c.-129-1516_-129-1515del	NP_001271245.1:n.-129-1516_-129-1515del
NM_174917.4:c.407_408del	NP_777577.2:p.Tyr136CysfsTer?
NR_104293.1:n.788_789del
XM_005256293.1:c.407_408del	XP_005256350.1:p.Tyr136CysfsTer?
XM_011522942.1:c.407_408del	XP_011521244.1:p.Tyr136CysfsTer?
XM_011522943.1:c.407_408del	XP_011521245.1:p.Tyr136CysfsTer?
XM_011522944.1:c.407_408del	XP_011521246.1:p.Tyr136CysfsTer?
XR_933238.1:n.751_752del
XR_933239.1:n.751_752del
XR_933240.1:n.751_752del
XR_933241.1:n.751_752del
NR_147928.1:n.788_789del
NR_147929.1:n.788_789del
XM_005256293.2:c.407_408del	XP_005256350.1:p.Tyr136CysfsTer?
XM_017023018.1:c.407_408del	XP_016878507.1:p.Tyr136CysfsTer?
XM_017023019.1:c.407_408del	XP_016878508.1:p.Tyr136CysfsTer?
XM_017023020.2:c.-4602_-4601del	XP_016878509.1:n.-4602_-4601del
XM_017023021.1:c.407_408del	XP_016878510.1:p.Tyr136CysfsTer?
XM_024450186.1:c.-129-1516_-129-1515del	XP_024305954.1:n.-129-1516_-129-1515del
XM_024450187.1:c.-129-1516_-129-1515del	XP_024305955.1:n.-129-1516_-129-1515del
XR_001751864.2:n.750_751del
XR_001751865.1:n.750_751del
XR_933238.2:n.750_751del
XR_933240.3:n.750_751del
NM_001127214.4:c.407_408del	NP_001120686.1:p.Tyr136CysfsTer?
NM_001243279.3:c.407_408del MANE Select	NP_001230208.1:p.Tyr136CysfsTer?
NM_001284316.2:c.-129-1516_-129-1515del	NP_001271245.1:n.-129-1516_-129-1515del
NM_174917.5:c.407_408del	NP_777577.2:p.Tyr136CysfsTer?
NR_104293.2:n.745_746del
NR_147928.2:n.745_746del
NR_147929.2:n.745_746del