Canonical Allele Identifier: CA397148242

Gene: ACSF3

Linked Data

• dbSNP Id: rs757673639
• MyVariant Identifiers: chr16:g.89211797C>G (hg19) ; chr16:g.89145389C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145389C>G , CM000678.2:g.89145389C>G	GRCh38
NC_000016.9:g.89211797C>G , CM000678.1:g.89211797C>G	GRCh37
NC_000016.8:g.87739298C>G	NCBI36
NG_031961.1:g.56581C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1489C>G	ENSP00000320646.4:p.Pro497Ala
ENST00000614302.5:c.1489C>G MANE Select	ENSP00000479130.1:p.Pro497Ala
ENST00000649953.1:c.1699C>G	ENSP00000497456.1:p.Pro567Ala
ENST00000317447.8:c.1489C>G	ENSP00000320646.4:p.Pro497Ala
ENST00000378345.8:c.694C>G	ENSP00000367596.4:p.Pro232Ala
ENST00000406948.7:c.1489C>G	ENSP00000384627.3:p.Pro497Ala
ENST00000537116.5:n.615C>G
ENST00000537155.1:n.229C>G
ENST00000542688.5:c.*233C>G	ENSP00000446281.1:n.*233C>G
ENST00000544543.5:c.694C>G	ENSP00000442781.1:p.Pro232Ala
ENST00000562204.1:n.462C>G
ENST00000614302.4:c.1489C>G	ENSP00000479130.1:p.Pro497Ala
NM_001127214.3:c.1489C>G	NP_001120686.1:p.Pro497Ala
NM_001243279.2:c.1489C>G	NP_001230208.1:p.Pro497Ala
NM_001284316.1:c.694C>G	NP_001271245.1:p.Pro232Ala
NM_174917.4:c.1489C>G	NP_777577.2:p.Pro497Ala
NR_045667.2:n.615C>G
NR_104293.1:n.1923C>G
XM_005256293.1:c.1489C>G	XP_005256350.1:p.Pro497Ala
XM_011522942.1:c.1489C>G	XP_011521244.1:p.Pro497Ala
XM_011522943.1:c.1489C>G	XP_011521245.1:p.Pro497Ala
XR_933239.1:n.1930C>G
XR_933240.1:n.1927C>G
XR_933241.1:n.1684C>G
NR_147928.1:n.1967C>G
NR_147929.1:n.1721C>G
XM_005256293.2:c.1489C>G	XP_005256350.1:p.Pro497Ala
XM_017023018.1:c.1489C>G	XP_016878507.1:p.Pro497Ala
XM_017023019.1:c.1489C>G	XP_016878508.1:p.Pro497Ala
XM_017023020.2:c.-3616C>G	XP_016878509.1:n.-3616C>G
XM_017023022.1:c.622C>G	XP_016878511.1:p.Pro208Ala
XM_024450186.1:c.694C>G	XP_024305954.1:p.Pro232Ala
XM_024450187.1:c.694C>G	XP_024305955.1:p.Pro232Ala
XR_001751864.2:n.1736C>G
XR_001751865.1:n.1683C>G
XR_933240.3:n.1926C>G
NM_001127214.4:c.1489C>G	NP_001120686.1:p.Pro497Ala
NM_001243279.3:c.1489C>G MANE Select	NP_001230208.1:p.Pro497Ala
NM_001284316.2:c.694C>G	NP_001271245.1:p.Pro232Ala
NM_174917.5:c.1489C>G	NP_777577.2:p.Pro497Ala
NR_104293.2:n.1880C>G
NR_147928.2:n.1924C>G
NR_147929.2:n.1678C>G