Canonical Allele Identifier: CA397147993

Gene: ACSF3

Linked Data

• MyVariant Identifiers: chr16:g.89211674G>T (hg19) ; chr16:g.89145266G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145266G>T , CM000678.2:g.89145266G>T	GRCh38
NC_000016.9:g.89211674G>T , CM000678.1:g.89211674G>T	GRCh37
NC_000016.8:g.87739175G>T	NCBI36
NG_031961.1:g.56458G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000317447.9:c.1367-1G>T	ENSP00000320646.4:n.1367-1G>T
ENST00000614302.5:c.1367-1G>T MANE Select	ENSP00000479130.1:n.1367-1G>T
ENST00000649953.1:c.1577-1G>T	ENSP00000497456.1:n.1577-1G>T
ENST00000317447.8:c.1367-1G>T	ENSP00000320646.4:n.1367-1G>T
ENST00000378345.8:c.572-1G>T	ENSP00000367596.4:n.572-1G>T
ENST00000406948.7:c.1367-1G>T	ENSP00000384627.3:n.1367-1G>T
ENST00000537116.5:n.493-1G>T
ENST00000537155.1:n.106G>T
ENST00000542688.5:c.*111-1G>T	ENSP00000446281.1:n.*111-1G>T
ENST00000544543.5:c.572-1G>T	ENSP00000442781.1:n.572-1G>T
ENST00000562204.1:n.339G>T
ENST00000614302.4:c.1367-1G>T	ENSP00000479130.1:n.1367-1G>T
NM_001127214.3:c.1367-1G>T	NP_001120686.1:n.1367-1G>T
NM_001243279.2:c.1367-1G>T	NP_001230208.1:n.1367-1G>T
NM_001284316.1:c.572-1G>T	NP_001271245.1:n.572-1G>T
NM_174917.4:c.1367-1G>T	NP_777577.2:n.1367-1G>T
NR_045667.2:n.493-1G>T
NR_104293.1:n.1800G>T
XM_005256293.1:c.1367-1G>T	XP_005256350.1:n.1367-1G>T
XM_011522942.1:c.1367-1G>T	XP_011521244.1:n.1367-1G>T
XM_011522943.1:c.1367-1G>T	XP_011521245.1:n.1367-1G>T
XR_933239.1:n.1808-1G>T
XR_933240.1:n.1805-1G>T
XR_933241.1:n.1562-1G>T
NR_147928.1:n.1845-1G>T
NR_147929.1:n.1599-1G>T
XM_005256293.2:c.1367-1G>T	XP_005256350.1:n.1367-1G>T
XM_017023018.1:c.1367-1G>T	XP_016878507.1:n.1367-1G>T
XM_017023019.1:c.1367-1G>T	XP_016878508.1:n.1367-1G>T
XM_017023020.2:c.-3739G>T	XP_016878509.1:n.-3739G>T
XM_017023022.1:c.500-1G>T	XP_016878511.1:n.500-1G>T
XM_024450186.1:c.572-1G>T	XP_024305954.1:n.572-1G>T
XM_024450187.1:c.572-1G>T	XP_024305955.1:n.572-1G>T
XR_001751864.2:n.1613G>T
XR_001751865.1:n.1561-1G>T
XR_933240.3:n.1804-1G>T
NM_001127214.4:c.1367-1G>T	NP_001120686.1:n.1367-1G>T
NM_001243279.3:c.1367-1G>T MANE Select	NP_001230208.1:n.1367-1G>T
NM_001284316.2:c.572-1G>T	NP_001271245.1:n.572-1G>T
NM_174917.5:c.1367-1G>T	NP_777577.2:n.1367-1G>T
NR_104293.2:n.1757G>T
NR_147928.2:n.1802-1G>T
NR_147929.2:n.1556-1G>T