Canonical Allele Identifier: CA397150719

Gene: ACSF3

Linked Data

• dbSNP Id: rs1401905863
• gnomAD v4: 16-89154161-G-T
• MyVariant Identifiers: chr16:g.89220569G>T (hg19) ; chr16:g.89154161G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154161G>T , CM000678.2:g.89154161G>T	GRCh38
NC_000016.9:g.89220569G>T , CM000678.1:g.89220569G>T	GRCh37
NC_000016.8:g.87748070G>T	NCBI36
NG_031961.1:g.65353G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1685G>T	ENSP00000320646.4:p.Gly562Val
ENST00000614302.5:c.1685G>T MANE Select	ENSP00000479130.1:p.Gly562Val
ENST00000649953.1:c.1895G>T	ENSP00000497456.1:p.Gly632Val
ENST00000317447.8:c.1685G>T	ENSP00000320646.4:p.Gly562Val
ENST00000378345.8:c.890G>T	ENSP00000367596.4:p.Gly297Val
ENST00000393145.5:n.6595G>T
ENST00000406948.7:c.1685G>T	ENSP00000384627.3:p.Gly562Val
ENST00000537116.5:n.811G>T
ENST00000537155.1:n.425G>T
ENST00000542688.5:c.*429G>T	ENSP00000446281.1:n.*429G>T
ENST00000614302.4:c.1685G>T	ENSP00000479130.1:p.Gly562Val
NM_001127214.3:c.1685G>T	NP_001120686.1:p.Gly562Val
NM_001243279.2:c.1685G>T	NP_001230208.1:p.Gly562Val
NM_001284316.1:c.890G>T	NP_001271245.1:p.Gly297Val
NM_174917.4:c.1685G>T	NP_777577.2:p.Gly562Val
NR_045667.2:n.811G>T
NR_104293.1:n.2119G>T
XR_933239.1:n.2126G>T
XR_933240.1:n.2123G>T
XR_933241.1:n.1880G>T
NR_147928.1:n.2163G>T
NR_147929.1:n.1917G>T
XM_017023020.2:c.-3420G>T	XP_016878509.1:n.-3420G>T
XM_024450187.1:c.890G>T	XP_024305955.1:p.Gly297Val
XR_001751864.2:n.1932G>T
XR_933240.3:n.2122G>T
NM_001127214.4:c.1685G>T	NP_001120686.1:p.Gly562Val
NM_001243279.3:c.1685G>T MANE Select	NP_001230208.1:p.Gly562Val
NM_001284316.2:c.890G>T	NP_001271245.1:p.Gly297Val
NM_174917.5:c.1685G>T	NP_777577.2:p.Gly562Val
NR_104293.2:n.2076G>T
NR_147928.2:n.2120G>T
NR_147929.2:n.1874G>T