Canonical Allele Identifier: CA2634920407

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89145124-TTGCCACAGGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145126_89145135del , CM000678.2:g.89145126_89145135del	GRCh38
NC_000016.9:g.89211534_89211543del , CM000678.1:g.89211534_89211543del	GRCh37
NC_000016.8:g.87739035_87739044del	NCBI36
NG_031961.1:g.56318_56327del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1367-141_1367-132del	ENSP00000320646.4:n.1367-141_1367-132del
ENST00000614302.5:c.1367-141_1367-132del MANE Select	ENSP00000479130.1:n.1367-141_1367-132del
ENST00000649953.1:c.1577-141_1577-132del	ENSP00000497456.1:n.1577-141_1577-132del
ENST00000317447.8:c.1367-141_1367-132del	ENSP00000320646.4:n.1367-141_1367-132del
ENST00000378345.8:c.572-141_572-132del	ENSP00000367596.4:n.572-141_572-132del
ENST00000406948.7:c.1367-141_1367-132del	ENSP00000384627.3:n.1367-141_1367-132del
ENST00000537116.5:n.493-141_493-132del
ENST00000542688.5:c.*111-141_*111-132del	ENSP00000446281.1:n.*111-141_*111-132del
ENST00000544543.5:c.572-141_572-132del	ENSP00000442781.1:n.572-141_572-132del
ENST00000562204.1:n.287-88_287-79del
ENST00000614302.4:c.1367-141_1367-132del	ENSP00000479130.1:n.1367-141_1367-132del
NM_001127214.3:c.1367-141_1367-132del	NP_001120686.1:n.1367-141_1367-132del
NM_001243279.2:c.1367-141_1367-132del	NP_001230208.1:n.1367-141_1367-132del
NM_001284316.1:c.572-141_572-132del	NP_001271245.1:n.572-141_572-132del
NM_174917.4:c.1367-141_1367-132del	NP_777577.2:n.1367-141_1367-132del
NR_045667.2:n.493-141_493-132del
NR_104293.1:n.1748-88_1748-79del
XM_005256293.1:c.1367-141_1367-132del	XP_005256350.1:n.1367-141_1367-132del
XM_011522942.1:c.1367-141_1367-132del	XP_011521244.1:n.1367-141_1367-132del
XM_011522943.1:c.1367-141_1367-132del	XP_011521245.1:n.1367-141_1367-132del
XR_933239.1:n.1808-141_1808-132del
XR_933240.1:n.1805-141_1805-132del
XR_933241.1:n.1562-141_1562-132del
NR_147928.1:n.1845-141_1845-132del
NR_147929.1:n.1599-141_1599-132del
XM_005256293.2:c.1367-141_1367-132del	XP_005256350.1:n.1367-141_1367-132del
XM_017023018.1:c.1367-141_1367-132del	XP_016878507.1:n.1367-141_1367-132del
XM_017023019.1:c.1367-141_1367-132del	XP_016878508.1:n.1367-141_1367-132del
XM_017023020.2:c.-3791-88_-3791-79del	XP_016878509.1:n.-3791-88_-3791-79del
XM_017023021.1:c.*5183_*5192del	XP_016878510.1:n.*5183_*5192del
XM_017023022.1:c.500-141_500-132del	XP_016878511.1:n.500-141_500-132del
XM_024450186.1:c.572-141_572-132del	XP_024305954.1:n.572-141_572-132del
XM_024450187.1:c.572-141_572-132del	XP_024305955.1:n.572-141_572-132del
XR_001751864.2:n.1561-88_1561-79del
XR_001751865.1:n.1561-141_1561-132del
XR_933238.2:n.5850_5859del
XR_933240.3:n.1804-141_1804-132del
NM_001127214.4:c.1367-141_1367-132del	NP_001120686.1:n.1367-141_1367-132del
NM_001243279.3:c.1367-141_1367-132del MANE Select	NP_001230208.1:n.1367-141_1367-132del
NM_001284316.2:c.572-141_572-132del	NP_001271245.1:n.572-141_572-132del
NM_174917.5:c.1367-141_1367-132del	NP_777577.2:n.1367-141_1367-132del
NR_104293.2:n.1705-88_1705-79del
NR_147928.2:n.1802-141_1802-132del
NR_147929.2:n.1556-141_1556-132del