Canonical Allele Identifier: CA497147167

Gene: ACSF3

Linked Data

• MyVariant Identifiers: chr16:g.89212407C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145999C>G , CM000678.2:g.89145999C>G	GRCh38
NC_000016.9:g.89212407C>G , CM000678.1:g.89212407C>G	GRCh37
NC_000016.8:g.87739908C>G	NCBI36
NG_031961.1:g.57191C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1563C>G	ENSP00000320646.4:p.Thr521=
ENST00000614302.5:c.1563C>G MANE Select	ENSP00000479130.1:p.Thr521=
ENST00000649953.1:c.1773C>G	ENSP00000497456.1:p.Thr591=
ENST00000317447.8:c.1563C>G	ENSP00000320646.4:p.Thr521=
ENST00000378345.8:c.768C>G	ENSP00000367596.4:p.Thr256=
ENST00000406948.7:c.1563C>G	ENSP00000384627.3:p.Thr521=
ENST00000535176.1:c.50C>G
ENST00000537116.5:n.689C>G
ENST00000537155.1:n.303C>G
ENST00000542688.5:c.*307C>G	ENSP00000446281.1:n.*307C>G
ENST00000562204.1:n.536C>G
ENST00000614302.4:c.1563C>G	ENSP00000479130.1:p.Thr521=
NM_001127214.3:c.1563C>G	NP_001120686.1:p.Thr521=
NM_001243279.2:c.1563C>G	NP_001230208.1:p.Thr521=
NM_001284316.1:c.768C>G	NP_001271245.1:p.Thr256=
NM_174917.4:c.1563C>G	NP_777577.2:p.Thr521=
NR_045667.2:n.689C>G
NR_104293.1:n.1997C>G
XM_005256293.1:c.1563C>G	XP_005256350.1:p.Thr521=
XM_011522942.1:c.1563C>G	XP_011521244.1:p.Thr521=
XM_011522943.1:c.1563C>G	XP_011521245.1:p.Thr521=
XR_933239.1:n.2004C>G
XR_933240.1:n.2001C>G
XR_933241.1:n.1758C>G
NR_147928.1:n.2041C>G
NR_147929.1:n.1795C>G
XM_005256293.2:c.1563C>G	XP_005256350.1:p.Thr521=
XM_017023018.1:c.1563C>G	XP_016878507.1:p.Thr521=
XM_017023019.1:c.1563C>G	XP_016878508.1:p.Thr521=
XM_017023020.2:c.-3542C>G	XP_016878509.1:n.-3542C>G
XM_017023022.1:c.696C>G	XP_016878511.1:p.Thr232=
XM_024450186.1:c.768C>G	XP_024305954.1:p.Thr256=
XM_024450187.1:c.768C>G	XP_024305955.1:p.Thr256=
XR_001751864.2:n.1810C>G
XR_001751865.1:n.1757C>G
XR_933240.3:n.2000C>G
NM_001127214.4:c.1563C>G	NP_001120686.1:p.Thr521=
NM_001243279.3:c.1563C>G MANE Select	NP_001230208.1:p.Thr521=
NM_001284316.2:c.768C>G	NP_001271245.1:p.Thr256=
NM_174917.5:c.1563C>G	NP_777577.2:p.Thr521=
NR_104293.2:n.1954C>G
NR_147928.2:n.1998C>G
NR_147929.2:n.1752C>G