Canonical Allele Identifier: CA397150992

Gene: ACSF3

Linked Data

• MyVariant Identifiers: chr16:g.89220611C>G (hg19) ; chr16:g.89154203C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154203C>G , CM000678.2:g.89154203C>G	GRCh38
NC_000016.9:g.89220611C>G , CM000678.1:g.89220611C>G	GRCh37
NC_000016.8:g.87748112C>G	NCBI36
NG_031961.1:g.65395C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1727C>G	ENSP00000320646.4:p.Ser576Ter
ENST00000614302.5:c.1727C>G MANE Select	ENSP00000479130.1:p.Ser576Ter
ENST00000649953.1:c.1937C>G	ENSP00000497456.1:p.Ser646Ter
ENST00000317447.8:c.1727C>G	ENSP00000320646.4:p.Ser576Ter
ENST00000378345.8:c.932C>G	ENSP00000367596.4:p.Ser311Ter
ENST00000393145.5:n.6637C>G
ENST00000406948.7:c.1727C>G	ENSP00000384627.3:p.Ser576Ter
ENST00000537116.5:n.853C>G
ENST00000537155.1:n.467C>G
ENST00000542688.5:c.*471C>G	ENSP00000446281.1:n.*471C>G
ENST00000614302.4:c.1727C>G	ENSP00000479130.1:p.Ser576Ter
NM_001127214.3:c.1727C>G	NP_001120686.1:p.Ser576Ter
NM_001243279.2:c.1727C>G	NP_001230208.1:p.Ser576Ter
NM_001284316.1:c.932C>G	NP_001271245.1:p.Ser311Ter
NM_174917.4:c.1727C>G	NP_777577.2:p.Ser576Ter
NR_045667.2:n.853C>G
NR_104293.1:n.2161C>G
XR_933239.1:n.2168C>G
XR_933240.1:n.2165C>G
XR_933241.1:n.1922C>G
NR_147928.1:n.2205C>G
NR_147929.1:n.1959C>G
XM_017023020.2:c.-3378C>G	XP_016878509.1:n.-3378C>G
XM_024450187.1:c.932C>G	XP_024305955.1:p.Ser311Ter
XR_001751864.2:n.1974C>G
XR_933240.3:n.2164C>G
NM_001127214.4:c.1727C>G	NP_001120686.1:p.Ser576Ter
NM_001243279.3:c.1727C>G MANE Select	NP_001230208.1:p.Ser576Ter
NM_001284316.2:c.932C>G	NP_001271245.1:p.Ser311Ter
NM_174917.5:c.1727C>G	NP_777577.2:p.Ser576Ter
NR_104293.2:n.2118C>G
NR_147928.2:n.2162C>G
NR_147929.2:n.1916C>G