Canonical Allele Identifier: CA397148256

Gene: ACSF3

Linked Data

• MyVariant Identifiers: chr16:g.89211804T>G (hg19) ; chr16:g.89145396T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145396T>G , CM000678.2:g.89145396T>G	GRCh38
NC_000016.9:g.89211804T>G , CM000678.1:g.89211804T>G	GRCh37
NC_000016.8:g.87739305T>G	NCBI36
NG_031961.1:g.56588T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1496T>G	ENSP00000320646.4:p.Ile499Ser
ENST00000614302.5:c.1496T>G MANE Select	ENSP00000479130.1:p.Ile499Ser
ENST00000649953.1:c.1706T>G	ENSP00000497456.1:p.Ile569Ser
ENST00000317447.8:c.1496T>G	ENSP00000320646.4:p.Ile499Ser
ENST00000378345.8:c.701T>G	ENSP00000367596.4:p.Ile234Ser
ENST00000406948.7:c.1496T>G	ENSP00000384627.3:p.Ile499Ser
ENST00000537116.5:n.622T>G
ENST00000537155.1:n.236T>G
ENST00000542688.5:c.*240T>G	ENSP00000446281.1:n.*240T>G
ENST00000544543.5:c.701T>G	ENSP00000442781.1:p.Ile234Ser
ENST00000562204.1:n.469T>G
ENST00000614302.4:c.1496T>G	ENSP00000479130.1:p.Ile499Ser
NM_001127214.3:c.1496T>G	NP_001120686.1:p.Ile499Ser
NM_001243279.2:c.1496T>G	NP_001230208.1:p.Ile499Ser
NM_001284316.1:c.701T>G	NP_001271245.1:p.Ile234Ser
NM_174917.4:c.1496T>G	NP_777577.2:p.Ile499Ser
NR_045667.2:n.622T>G
NR_104293.1:n.1930T>G
XM_005256293.1:c.1496T>G	XP_005256350.1:p.Ile499Ser
XM_011522942.1:c.1496T>G	XP_011521244.1:p.Ile499Ser
XM_011522943.1:c.1496T>G	XP_011521245.1:p.Ile499Ser
XR_933239.1:n.1937T>G
XR_933240.1:n.1934T>G
XR_933241.1:n.1691T>G
NR_147928.1:n.1974T>G
NR_147929.1:n.1728T>G
XM_005256293.2:c.1496T>G	XP_005256350.1:p.Ile499Ser
XM_017023018.1:c.1496T>G	XP_016878507.1:p.Ile499Ser
XM_017023019.1:c.1496T>G	XP_016878508.1:p.Ile499Ser
XM_017023020.2:c.-3609T>G	XP_016878509.1:n.-3609T>G
XM_017023022.1:c.629T>G	XP_016878511.1:p.Ile210Ser
XM_024450186.1:c.701T>G	XP_024305954.1:p.Ile234Ser
XM_024450187.1:c.701T>G	XP_024305955.1:p.Ile234Ser
XR_001751864.2:n.1743T>G
XR_001751865.1:n.1690T>G
XR_933240.3:n.1933T>G
NM_001127214.4:c.1496T>G	NP_001120686.1:p.Ile499Ser
NM_001243279.3:c.1496T>G MANE Select	NP_001230208.1:p.Ile499Ser
NM_001284316.2:c.701T>G	NP_001271245.1:p.Ile234Ser
NM_174917.5:c.1496T>G	NP_777577.2:p.Ile499Ser
NR_104293.2:n.1887T>G
NR_147928.2:n.1931T>G
NR_147929.2:n.1685T>G