Canonical Allele Identifier: CA397148090

Gene: ACSF3

Linked Data

• MyVariant Identifiers: chr16:g.89211723C>G (hg19) ; chr16:g.89145315C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145315C>G , CM000678.2:g.89145315C>G	GRCh38
NC_000016.9:g.89211723C>G , CM000678.1:g.89211723C>G	GRCh37
NC_000016.8:g.87739224C>G	NCBI36
NG_031961.1:g.56507C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000317447.9:c.1415C>G	ENSP00000320646.4:p.Thr472Ser
ENST00000614302.5:c.1415C>G MANE Select	ENSP00000479130.1:p.Thr472Ser
ENST00000649953.1:c.1625C>G	ENSP00000497456.1:p.Thr542Ser
ENST00000317447.8:c.1415C>G	ENSP00000320646.4:p.Thr472Ser
ENST00000378345.8:c.620C>G	ENSP00000367596.4:p.Thr207Ser
ENST00000406948.7:c.1415C>G	ENSP00000384627.3:p.Thr472Ser
ENST00000537116.5:n.541C>G
ENST00000537155.1:n.155C>G
ENST00000542688.5:c.*159C>G	ENSP00000446281.1:n.*159C>G
ENST00000544543.5:c.620C>G	ENSP00000442781.1:p.Thr207Ser
ENST00000562204.1:n.388C>G
ENST00000614302.4:c.1415C>G	ENSP00000479130.1:p.Thr472Ser
NM_001127214.3:c.1415C>G	NP_001120686.1:p.Thr472Ser
NM_001243279.2:c.1415C>G	NP_001230208.1:p.Thr472Ser
NM_001284316.1:c.620C>G	NP_001271245.1:p.Thr207Ser
NM_174917.4:c.1415C>G	NP_777577.2:p.Thr472Ser
NR_045667.2:n.541C>G
NR_104293.1:n.1849C>G
XM_005256293.1:c.1415C>G	XP_005256350.1:p.Thr472Ser
XM_011522942.1:c.1415C>G	XP_011521244.1:p.Thr472Ser
XM_011522943.1:c.1415C>G	XP_011521245.1:p.Thr472Ser
XR_933239.1:n.1856C>G
XR_933240.1:n.1853C>G
XR_933241.1:n.1610C>G
NR_147928.1:n.1893C>G
NR_147929.1:n.1647C>G
XM_005256293.2:c.1415C>G	XP_005256350.1:p.Thr472Ser
XM_017023018.1:c.1415C>G	XP_016878507.1:p.Thr472Ser
XM_017023019.1:c.1415C>G	XP_016878508.1:p.Thr472Ser
XM_017023020.2:c.-3690C>G	XP_016878509.1:n.-3690C>G
XM_017023022.1:c.548C>G	XP_016878511.1:p.Thr183Ser
XM_024450186.1:c.620C>G	XP_024305954.1:p.Thr207Ser
XM_024450187.1:c.620C>G	XP_024305955.1:p.Thr207Ser
XR_001751864.2:n.1662C>G
XR_001751865.1:n.1609C>G
XR_933240.3:n.1852C>G
NM_001127214.4:c.1415C>G	NP_001120686.1:p.Thr472Ser
NM_001243279.3:c.1415C>G MANE Select	NP_001230208.1:p.Thr472Ser
NM_001284316.2:c.620C>G	NP_001271245.1:p.Thr207Ser
NM_174917.5:c.1415C>G	NP_777577.2:p.Thr472Ser
NR_104293.2:n.1806C>G
NR_147928.2:n.1850C>G
NR_147929.2:n.1604C>G