Canonical Allele Identifier: CA397150880

Gene: ACSF3

Linked Data

• MyVariant Identifiers: chr16:g.89220593T>G (hg19) ; chr16:g.89154185T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154185T>G , CM000678.2:g.89154185T>G	GRCh38
NC_000016.9:g.89220593T>G , CM000678.1:g.89220593T>G	GRCh37
NC_000016.8:g.87748094T>G	NCBI36
NG_031961.1:g.65377T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1709T>G	ENSP00000320646.4:p.Ile570Ser
ENST00000614302.5:c.1709T>G MANE Select	ENSP00000479130.1:p.Ile570Ser
ENST00000649953.1:c.1919T>G	ENSP00000497456.1:p.Ile640Ser
ENST00000317447.8:c.1709T>G	ENSP00000320646.4:p.Ile570Ser
ENST00000378345.8:c.914T>G	ENSP00000367596.4:p.Ile305Ser
ENST00000393145.5:n.6619T>G
ENST00000406948.7:c.1709T>G	ENSP00000384627.3:p.Ile570Ser
ENST00000537116.5:n.835T>G
ENST00000537155.1:n.449T>G
ENST00000542688.5:c.*453T>G	ENSP00000446281.1:n.*453T>G
ENST00000614302.4:c.1709T>G	ENSP00000479130.1:p.Ile570Ser
NM_001127214.3:c.1709T>G	NP_001120686.1:p.Ile570Ser
NM_001243279.2:c.1709T>G	NP_001230208.1:p.Ile570Ser
NM_001284316.1:c.914T>G	NP_001271245.1:p.Ile305Ser
NM_174917.4:c.1709T>G	NP_777577.2:p.Ile570Ser
NR_045667.2:n.835T>G
NR_104293.1:n.2143T>G
XR_933239.1:n.2150T>G
XR_933240.1:n.2147T>G
XR_933241.1:n.1904T>G
NR_147928.1:n.2187T>G
NR_147929.1:n.1941T>G
XM_017023020.2:c.-3396T>G	XP_016878509.1:n.-3396T>G
XM_024450187.1:c.914T>G	XP_024305955.1:p.Ile305Ser
XR_001751864.2:n.1956T>G
XR_933240.3:n.2146T>G
NM_001127214.4:c.1709T>G	NP_001120686.1:p.Ile570Ser
NM_001243279.3:c.1709T>G MANE Select	NP_001230208.1:p.Ile570Ser
NM_001284316.2:c.914T>G	NP_001271245.1:p.Ile305Ser
NM_174917.5:c.1709T>G	NP_777577.2:p.Ile570Ser
NR_104293.2:n.2100T>G
NR_147928.2:n.2144T>G
NR_147929.2:n.1898T>G