Canonical Allele Identifier: CA2634917564

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89100618-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89100621del , CM000678.2:g.89100621del	GRCh38
NC_000016.9:g.89167029del , CM000678.1:g.89167029del	GRCh37
NC_000016.8:g.87694530del	NCBI36
NG_031961.1:g.11813del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.-20-41del	ENSP00000320646.4:n.-20-41del
ENST00000614302.5:c.-20-41del MANE Select	ENSP00000479130.1:n.-20-41del
ENST00000317447.8:c.-20-41del	ENSP00000320646.4:n.-20-41del
ENST00000378345.8:c.-129-1983del	ENSP00000367596.4:n.-129-1983del
ENST00000406948.7:c.-20-41del	ENSP00000384627.3:n.-20-41del
ENST00000537290.5:c.-20-41del	ENSP00000440734.1:n.-20-41del
ENST00000537895.5:c.-129-1983del	ENSP00000439201.1:n.-129-1983del
ENST00000540697.5:c.-129-1983del	ENSP00000445397.1:n.-129-1983del
ENST00000541755.2:c.-20-41del	ENSP00000457301.1:n.-20-41del
ENST00000542688.5:c.-56-5del	ENSP00000446281.1:n.-56-5del
ENST00000614302.4:c.-20-41del	ENSP00000479130.1:n.-20-41del
NM_001127214.3:c.-20-41del	NP_001120686.1:n.-20-41del
NM_001243279.2:c.-20-41del	NP_001230208.1:n.-20-41del
NM_001284316.1:c.-129-1983del	NP_001271245.1:n.-129-1983del
NM_174917.4:c.-20-41del	NP_777577.2:n.-20-41del
NR_104293.1:n.362-41del
XM_005256293.1:c.-20-41del	XP_005256350.1:n.-20-41del
XM_011522942.1:c.-20-41del	XP_011521244.1:n.-20-41del
XM_011522943.1:c.-20-41del	XP_011521245.1:n.-20-41del
XM_011522944.1:c.-20-41del	XP_011521246.1:n.-20-41del
XR_933238.1:n.325-41del
XR_933239.1:n.325-41del
XR_933240.1:n.325-41del
XR_933241.1:n.325-41del
NR_147928.1:n.362-41del
NR_147929.1:n.362-41del
XM_005256293.2:c.-20-41del	XP_005256350.1:n.-20-41del
XM_017023018.1:c.-20-41del	XP_016878507.1:n.-20-41del
XM_017023019.1:c.-20-41del	XP_016878508.1:n.-20-41del
XM_017023021.1:c.-20-41del	XP_016878510.1:n.-20-41del
XM_024450186.1:c.-129-1983del	XP_024305954.1:n.-129-1983del
XM_024450187.1:c.-129-1983del	XP_024305955.1:n.-129-1983del
XR_001751864.2:n.324-41del
XR_001751865.1:n.324-41del
XR_933238.2:n.324-41del
XR_933240.3:n.324-41del
NM_001127214.4:c.-20-41del	NP_001120686.1:n.-20-41del
NM_001243279.3:c.-20-41del MANE Select	NP_001230208.1:n.-20-41del
NM_001284316.2:c.-129-1983del	NP_001271245.1:n.-129-1983del
NM_174917.5:c.-20-41del	NP_777577.2:n.-20-41del
NR_104293.2:n.319-41del
NR_147928.2:n.319-41del
NR_147929.2:n.319-41del