Canonical Allele Identifier: CA397148196

Gene: ACSF3

Linked Data

• MyVariant Identifiers: chr16:g.89211774T>C (hg19) ; chr16:g.89145366T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145366T>C , CM000678.2:g.89145366T>C	GRCh38
NC_000016.9:g.89211774T>C , CM000678.1:g.89211774T>C	GRCh37
NC_000016.8:g.87739275T>C	NCBI36
NG_031961.1:g.56558T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1466T>C	ENSP00000320646.4:p.Val489Ala
ENST00000614302.5:c.1466T>C MANE Select	ENSP00000479130.1:p.Val489Ala
ENST00000649953.1:c.1676T>C	ENSP00000497456.1:p.Val559Ala
ENST00000317447.8:c.1466T>C	ENSP00000320646.4:p.Val489Ala
ENST00000378345.8:c.671T>C	ENSP00000367596.4:p.Val224Ala
ENST00000406948.7:c.1466T>C	ENSP00000384627.3:p.Val489Ala
ENST00000537116.5:n.592T>C
ENST00000537155.1:n.206T>C
ENST00000542688.5:c.*210T>C	ENSP00000446281.1:n.*210T>C
ENST00000544543.5:c.671T>C	ENSP00000442781.1:p.Val224Ala
ENST00000562204.1:n.439T>C
ENST00000614302.4:c.1466T>C	ENSP00000479130.1:p.Val489Ala
NM_001127214.3:c.1466T>C	NP_001120686.1:p.Val489Ala
NM_001243279.2:c.1466T>C	NP_001230208.1:p.Val489Ala
NM_001284316.1:c.671T>C	NP_001271245.1:p.Val224Ala
NM_174917.4:c.1466T>C	NP_777577.2:p.Val489Ala
NR_045667.2:n.592T>C
NR_104293.1:n.1900T>C
XM_005256293.1:c.1466T>C	XP_005256350.1:p.Val489Ala
XM_011522942.1:c.1466T>C	XP_011521244.1:p.Val489Ala
XM_011522943.1:c.1466T>C	XP_011521245.1:p.Val489Ala
XR_933239.1:n.1907T>C
XR_933240.1:n.1904T>C
XR_933241.1:n.1661T>C
NR_147928.1:n.1944T>C
NR_147929.1:n.1698T>C
XM_005256293.2:c.1466T>C	XP_005256350.1:p.Val489Ala
XM_017023018.1:c.1466T>C	XP_016878507.1:p.Val489Ala
XM_017023019.1:c.1466T>C	XP_016878508.1:p.Val489Ala
XM_017023020.2:c.-3639T>C	XP_016878509.1:n.-3639T>C
XM_017023022.1:c.599T>C	XP_016878511.1:p.Val200Ala
XM_024450186.1:c.671T>C	XP_024305954.1:p.Val224Ala
XM_024450187.1:c.671T>C	XP_024305955.1:p.Val224Ala
XR_001751864.2:n.1713T>C
XR_001751865.1:n.1660T>C
XR_933240.3:n.1903T>C
NM_001127214.4:c.1466T>C	NP_001120686.1:p.Val489Ala
NM_001243279.3:c.1466T>C MANE Select	NP_001230208.1:p.Val489Ala
NM_001284316.2:c.671T>C	NP_001271245.1:p.Val224Ala
NM_174917.5:c.1466T>C	NP_777577.2:p.Val489Ala
NR_104293.2:n.1857T>C
NR_147928.2:n.1901T>C
NR_147929.2:n.1655T>C