Canonical Allele Identifier: CA2241515267

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145092_89145097delinsGCTTAC , CM000678.2:g.89145092_89145097delinsGCTTAC	GRCh38
NC_000016.9:g.89211500_89211505delinsGCTTAC , CM000678.1:g.89211500_89211505delinsGCTTAC	GRCh37
NC_000016.8:g.87739001_87739006delinsGCTTAC	NCBI36
NG_031961.1:g.56284_56289delinsGCTTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1367-175_1367-170delinsGCTTAC	ENSP00000320646.4:n.1367-175_1367-170delinsGCTTAC
ENST00000614302.5:c.1367-175_1367-170delinsGCTTAC MANE Select	ENSP00000479130.1:n.1367-175_1367-170delinsGCTTAC
ENST00000649953.1:c.1577-175_1577-170delinsGCTTAC	ENSP00000497456.1:n.1577-175_1577-170delinsGCTTAC
ENST00000317447.8:c.1367-175_1367-170delinsGCTTAC	ENSP00000320646.4:n.1367-175_1367-170delinsGCTTAC
ENST00000378345.8:c.572-175_572-170delinsGCTTAC	ENSP00000367596.4:n.572-175_572-170delinsGCTTAC
ENST00000406948.7:c.1367-175_1367-170delinsGCTTAC	ENSP00000384627.3:n.1367-175_1367-170delinsGCTTAC
ENST00000537116.5:n.493-175_493-170delinsGCTTAC
ENST00000542688.5:c.*111-175_*111-170delinsGCTTAC	ENSP00000446281.1:n.*111-175_*111-170delinsGCTTAC
ENST00000544543.5:c.572-175_572-170delinsGCTTAC	ENSP00000442781.1:n.572-175_572-170delinsGCTTAC
ENST00000562204.1:n.287-122_287-117delinsGCTTAC
ENST00000614302.4:c.1367-175_1367-170delinsGCTTAC	ENSP00000479130.1:n.1367-175_1367-170delinsGCTTAC
NM_001127214.3:c.1367-175_1367-170delinsGCTTAC	NP_001120686.1:n.1367-175_1367-170delinsGCTTAC
NM_001243279.2:c.1367-175_1367-170delinsGCTTAC	NP_001230208.1:n.1367-175_1367-170delinsGCTTAC
NM_001284316.1:c.572-175_572-170delinsGCTTAC	NP_001271245.1:n.572-175_572-170delinsGCTTAC
NM_174917.4:c.1367-175_1367-170delinsGCTTAC	NP_777577.2:n.1367-175_1367-170delinsGCTTAC
NR_045667.2:n.493-175_493-170delinsGCTTAC
NR_104293.1:n.1748-122_1748-117delinsGCTTAC
XM_005256293.1:c.1367-175_1367-170delinsGCTTAC	XP_005256350.1:n.1367-175_1367-170delinsGCTTAC
XM_011522942.1:c.1367-175_1367-170delinsGCTTAC	XP_011521244.1:n.1367-175_1367-170delinsGCTTAC
XM_011522943.1:c.1367-175_1367-170delinsGCTTAC	XP_011521245.1:n.1367-175_1367-170delinsGCTTAC
XR_933239.1:n.1808-175_1808-170delinsGCTTAC
XR_933240.1:n.1805-175_1805-170delinsGCTTAC
XR_933241.1:n.1562-175_1562-170delinsGCTTAC
NR_147928.1:n.1845-175_1845-170delinsGCTTAC
NR_147929.1:n.1599-175_1599-170delinsGCTTAC
XM_005256293.2:c.1367-175_1367-170delinsGCTTAC	XP_005256350.1:n.1367-175_1367-170delinsGCTTAC
XM_017023018.1:c.1367-175_1367-170delinsGCTTAC	XP_016878507.1:n.1367-175_1367-170delinsGCTTAC
XM_017023019.1:c.1367-175_1367-170delinsGCTTAC	XP_016878508.1:n.1367-175_1367-170delinsGCTTAC
XM_017023020.2:c.-3791-122_-3791-117delinsGCTTAC	XP_016878509.1:n.-3791-122_-3791-117delinsGCTTAC
XM_017023021.1:c.*5149_*5154delinsGCTTAC	XP_016878510.1:n.*5149_*5154delinsGCTTAC
XM_017023022.1:c.500-175_500-170delinsGCTTAC	XP_016878511.1:n.500-175_500-170delinsGCTTAC
XM_024450186.1:c.572-175_572-170delinsGCTTAC	XP_024305954.1:n.572-175_572-170delinsGCTTAC
XM_024450187.1:c.572-175_572-170delinsGCTTAC	XP_024305955.1:n.572-175_572-170delinsGCTTAC
XR_001751864.2:n.1561-122_1561-117delinsGCTTAC
XR_001751865.1:n.1561-175_1561-170delinsGCTTAC
XR_933238.2:n.5816_5821delinsGCTTAC
XR_933240.3:n.1804-175_1804-170delinsGCTTAC
NM_001127214.4:c.1367-175_1367-170delinsGCTTAC	NP_001120686.1:n.1367-175_1367-170delinsGCTTAC
NM_001243279.3:c.1367-175_1367-170delinsGCTTAC MANE Select	NP_001230208.1:n.1367-175_1367-170delinsGCTTAC
NM_001284316.2:c.572-175_572-170delinsGCTTAC	NP_001271245.1:n.572-175_572-170delinsGCTTAC
NM_174917.5:c.1367-175_1367-170delinsGCTTAC	NP_777577.2:n.1367-175_1367-170delinsGCTTAC
NR_104293.2:n.1705-122_1705-117delinsGCTTAC
NR_147928.2:n.1802-175_1802-170delinsGCTTAC
NR_147929.2:n.1556-175_1556-170delinsGCTTAC