Canonical Allele Identifier: CA2634920425

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89145144-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145144G>A , CM000678.2:g.89145144G>A	GRCh38
NC_000016.9:g.89211552G>A , CM000678.1:g.89211552G>A	GRCh37
NC_000016.8:g.87739053G>A	NCBI36
NG_031961.1:g.56336G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1367-123G>A	ENSP00000320646.4:n.1367-123G>A
ENST00000614302.5:c.1367-123G>A MANE Select	ENSP00000479130.1:n.1367-123G>A
ENST00000649953.1:c.1577-123G>A	ENSP00000497456.1:n.1577-123G>A
ENST00000317447.8:c.1367-123G>A	ENSP00000320646.4:n.1367-123G>A
ENST00000378345.8:c.572-123G>A	ENSP00000367596.4:n.572-123G>A
ENST00000406948.7:c.1367-123G>A	ENSP00000384627.3:n.1367-123G>A
ENST00000537116.5:n.493-123G>A
ENST00000542688.5:c.*111-123G>A	ENSP00000446281.1:n.*111-123G>A
ENST00000544543.5:c.572-123G>A	ENSP00000442781.1:n.572-123G>A
ENST00000562204.1:n.287-70G>A
ENST00000614302.4:c.1367-123G>A	ENSP00000479130.1:n.1367-123G>A
NM_001127214.3:c.1367-123G>A	NP_001120686.1:n.1367-123G>A
NM_001243279.2:c.1367-123G>A	NP_001230208.1:n.1367-123G>A
NM_001284316.1:c.572-123G>A	NP_001271245.1:n.572-123G>A
NM_174917.4:c.1367-123G>A	NP_777577.2:n.1367-123G>A
NR_045667.2:n.493-123G>A
NR_104293.1:n.1748-70G>A
XM_005256293.1:c.1367-123G>A	XP_005256350.1:n.1367-123G>A
XM_011522942.1:c.1367-123G>A	XP_011521244.1:n.1367-123G>A
XM_011522943.1:c.1367-123G>A	XP_011521245.1:n.1367-123G>A
XR_933239.1:n.1808-123G>A
XR_933240.1:n.1805-123G>A
XR_933241.1:n.1562-123G>A
NR_147928.1:n.1845-123G>A
NR_147929.1:n.1599-123G>A
XM_005256293.2:c.1367-123G>A	XP_005256350.1:n.1367-123G>A
XM_017023018.1:c.1367-123G>A	XP_016878507.1:n.1367-123G>A
XM_017023019.1:c.1367-123G>A	XP_016878508.1:n.1367-123G>A
XM_017023020.2:c.-3791-70G>A	XP_016878509.1:n.-3791-70G>A
XM_017023021.1:c.*5201G>A	XP_016878510.1:n.*5201G>A
XM_017023022.1:c.500-123G>A	XP_016878511.1:n.500-123G>A
XM_024450186.1:c.572-123G>A	XP_024305954.1:n.572-123G>A
XM_024450187.1:c.572-123G>A	XP_024305955.1:n.572-123G>A
XR_001751864.2:n.1561-70G>A
XR_001751865.1:n.1561-123G>A
XR_933238.2:n.5868G>A
XR_933240.3:n.1804-123G>A
NM_001127214.4:c.1367-123G>A	NP_001120686.1:n.1367-123G>A
NM_001243279.3:c.1367-123G>A MANE Select	NP_001230208.1:n.1367-123G>A
NM_001284316.2:c.572-123G>A	NP_001271245.1:n.572-123G>A
NM_174917.5:c.1367-123G>A	NP_777577.2:n.1367-123G>A
NR_104293.2:n.1705-70G>A
NR_147928.2:n.1802-123G>A
NR_147929.2:n.1556-123G>A