Canonical Allele Identifier: CA397148088

Gene: ACSF3

Linked Data

• MyVariant Identifiers: chr16:g.89211722A>G (hg19) ; chr16:g.89145314A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145314A>G , CM000678.2:g.89145314A>G	GRCh38
NC_000016.9:g.89211722A>G , CM000678.1:g.89211722A>G	GRCh37
NC_000016.8:g.87739223A>G	NCBI36
NG_031961.1:g.56506A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000317447.9:c.1414A>G	ENSP00000320646.4:p.Thr472Ala
ENST00000614302.5:c.1414A>G MANE Select	ENSP00000479130.1:p.Thr472Ala
ENST00000649953.1:c.1624A>G	ENSP00000497456.1:p.Thr542Ala
ENST00000317447.8:c.1414A>G	ENSP00000320646.4:p.Thr472Ala
ENST00000378345.8:c.619A>G	ENSP00000367596.4:p.Thr207Ala
ENST00000406948.7:c.1414A>G	ENSP00000384627.3:p.Thr472Ala
ENST00000537116.5:n.540A>G
ENST00000537155.1:n.154A>G
ENST00000542688.5:c.*158A>G	ENSP00000446281.1:n.*158A>G
ENST00000544543.5:c.619A>G	ENSP00000442781.1:p.Thr207Ala
ENST00000562204.1:n.387A>G
ENST00000614302.4:c.1414A>G	ENSP00000479130.1:p.Thr472Ala
NM_001127214.3:c.1414A>G	NP_001120686.1:p.Thr472Ala
NM_001243279.2:c.1414A>G	NP_001230208.1:p.Thr472Ala
NM_001284316.1:c.619A>G	NP_001271245.1:p.Thr207Ala
NM_174917.4:c.1414A>G	NP_777577.2:p.Thr472Ala
NR_045667.2:n.540A>G
NR_104293.1:n.1848A>G
XM_005256293.1:c.1414A>G	XP_005256350.1:p.Thr472Ala
XM_011522942.1:c.1414A>G	XP_011521244.1:p.Thr472Ala
XM_011522943.1:c.1414A>G	XP_011521245.1:p.Thr472Ala
XR_933239.1:n.1855A>G
XR_933240.1:n.1852A>G
XR_933241.1:n.1609A>G
NR_147928.1:n.1892A>G
NR_147929.1:n.1646A>G
XM_005256293.2:c.1414A>G	XP_005256350.1:p.Thr472Ala
XM_017023018.1:c.1414A>G	XP_016878507.1:p.Thr472Ala
XM_017023019.1:c.1414A>G	XP_016878508.1:p.Thr472Ala
XM_017023020.2:c.-3691A>G	XP_016878509.1:n.-3691A>G
XM_017023022.1:c.547A>G	XP_016878511.1:p.Thr183Ala
XM_024450186.1:c.619A>G	XP_024305954.1:p.Thr207Ala
XM_024450187.1:c.619A>G	XP_024305955.1:p.Thr207Ala
XR_001751864.2:n.1661A>G
XR_001751865.1:n.1608A>G
XR_933240.3:n.1851A>G
NM_001127214.4:c.1414A>G	NP_001120686.1:p.Thr472Ala
NM_001243279.3:c.1414A>G MANE Select	NP_001230208.1:p.Thr472Ala
NM_001284316.2:c.619A>G	NP_001271245.1:p.Thr207Ala
NM_174917.5:c.1414A>G	NP_777577.2:p.Thr472Ala
NR_104293.2:n.1805A>G
NR_147928.2:n.1849A>G
NR_147929.2:n.1603A>G