Canonical Allele Identifier: CA2634920474

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89145416-TTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145417_89145418del , CM000678.2:g.89145417_89145418del	GRCh38
NC_000016.9:g.89211825_89211826del , CM000678.1:g.89211825_89211826del	GRCh37
NC_000016.8:g.87739326_87739327del	NCBI36
NG_031961.1:g.56609_56610del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1501+16_1501+17del	ENSP00000320646.4:n.1501+16_1501+17del
ENST00000614302.5:c.1501+16_1501+17del MANE Select	ENSP00000479130.1:n.1501+16_1501+17del
ENST00000649953.1:c.1711+16_1711+17del	ENSP00000497456.1:n.1711+16_1711+17del
ENST00000317447.8:c.1501+16_1501+17del	ENSP00000320646.4:n.1501+16_1501+17del
ENST00000378345.8:c.706+16_706+17del	ENSP00000367596.4:n.706+16_706+17del
ENST00000406948.7:c.1501+16_1501+17del	ENSP00000384627.3:n.1501+16_1501+17del
ENST00000537116.5:n.627+16_627+17del
ENST00000537155.1:n.241+16_241+17del
ENST00000542688.5:c.*245+16_*245+17del	ENSP00000446281.1:n.*245+16_*245+17del
ENST00000562204.1:n.474+16_474+17del
ENST00000614302.4:c.1501+16_1501+17del	ENSP00000479130.1:n.1501+16_1501+17del
NM_001127214.3:c.1501+16_1501+17del	NP_001120686.1:n.1501+16_1501+17del
NM_001243279.2:c.1501+16_1501+17del	NP_001230208.1:n.1501+16_1501+17del
NM_001284316.1:c.706+16_706+17del	NP_001271245.1:n.706+16_706+17del
NM_174917.4:c.1501+16_1501+17del	NP_777577.2:n.1501+16_1501+17del
NR_045667.2:n.627+16_627+17del
NR_104293.1:n.1935+16_1935+17del
XM_005256293.1:c.1501+16_1501+17del	XP_005256350.1:n.1501+16_1501+17del
XM_011522942.1:c.1501+16_1501+17del	XP_011521244.1:n.1501+16_1501+17del
XM_011522943.1:c.1501+16_1501+17del	XP_011521245.1:n.1501+16_1501+17del
XR_933239.1:n.1942+16_1942+17del
XR_933240.1:n.1939+16_1939+17del
XR_933241.1:n.1696+16_1696+17del
NR_147928.1:n.1979+16_1979+17del
NR_147929.1:n.1733+16_1733+17del
XM_005256293.2:c.1501+16_1501+17del	XP_005256350.1:n.1501+16_1501+17del
XM_017023018.1:c.1501+16_1501+17del	XP_016878507.1:n.1501+16_1501+17del
XM_017023019.1:c.1501+16_1501+17del	XP_016878508.1:n.1501+16_1501+17del
XM_017023020.2:c.-3604+16_-3604+17del	XP_016878509.1:n.-3604+16_-3604+17del
XM_017023022.1:c.634+16_634+17del	XP_016878511.1:n.634+16_634+17del
XM_024450186.1:c.706+16_706+17del	XP_024305954.1:n.706+16_706+17del
XM_024450187.1:c.706+16_706+17del	XP_024305955.1:n.706+16_706+17del
XR_001751864.2:n.1748+16_1748+17del
XR_001751865.1:n.1695+16_1695+17del
XR_933240.3:n.1938+16_1938+17del
NM_001127214.4:c.1501+16_1501+17del	NP_001120686.1:n.1501+16_1501+17del
NM_001243279.3:c.1501+16_1501+17del MANE Select	NP_001230208.1:n.1501+16_1501+17del
NM_001284316.2:c.706+16_706+17del	NP_001271245.1:n.706+16_706+17del
NM_174917.5:c.1501+16_1501+17del	NP_777577.2:n.1501+16_1501+17del
NR_104293.2:n.1892+16_1892+17del
NR_147928.2:n.1936+16_1936+17del
NR_147929.2:n.1690+16_1690+17del