Canonical Allele Identifier: CA397148121

Gene: ACSF3

Linked Data

• MyVariant Identifiers: chr16:g.89211738T>C (hg19) ; chr16:g.89145330T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145330T>C , CM000678.2:g.89145330T>C	GRCh38
NC_000016.9:g.89211738T>C , CM000678.1:g.89211738T>C	GRCh37
NC_000016.8:g.87739239T>C	NCBI36
NG_031961.1:g.56522T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1430T>C	ENSP00000320646.4:p.Ile477Thr
ENST00000614302.5:c.1430T>C MANE Select	ENSP00000479130.1:p.Ile477Thr
ENST00000649953.1:c.1640T>C	ENSP00000497456.1:p.Ile547Thr
ENST00000317447.8:c.1430T>C	ENSP00000320646.4:p.Ile477Thr
ENST00000378345.8:c.635T>C	ENSP00000367596.4:p.Ile212Thr
ENST00000406948.7:c.1430T>C	ENSP00000384627.3:p.Ile477Thr
ENST00000537116.5:n.556T>C
ENST00000537155.1:n.170T>C
ENST00000542688.5:c.*174T>C	ENSP00000446281.1:n.*174T>C
ENST00000544543.5:c.635T>C	ENSP00000442781.1:p.Ile212Thr
ENST00000562204.1:n.403T>C
ENST00000614302.4:c.1430T>C	ENSP00000479130.1:p.Ile477Thr
NM_001127214.3:c.1430T>C	NP_001120686.1:p.Ile477Thr
NM_001243279.2:c.1430T>C	NP_001230208.1:p.Ile477Thr
NM_001284316.1:c.635T>C	NP_001271245.1:p.Ile212Thr
NM_174917.4:c.1430T>C	NP_777577.2:p.Ile477Thr
NR_045667.2:n.556T>C
NR_104293.1:n.1864T>C
XM_005256293.1:c.1430T>C	XP_005256350.1:p.Ile477Thr
XM_011522942.1:c.1430T>C	XP_011521244.1:p.Ile477Thr
XM_011522943.1:c.1430T>C	XP_011521245.1:p.Ile477Thr
XR_933239.1:n.1871T>C
XR_933240.1:n.1868T>C
XR_933241.1:n.1625T>C
NR_147928.1:n.1908T>C
NR_147929.1:n.1662T>C
XM_005256293.2:c.1430T>C	XP_005256350.1:p.Ile477Thr
XM_017023018.1:c.1430T>C	XP_016878507.1:p.Ile477Thr
XM_017023019.1:c.1430T>C	XP_016878508.1:p.Ile477Thr
XM_017023020.2:c.-3675T>C	XP_016878509.1:n.-3675T>C
XM_017023022.1:c.563T>C	XP_016878511.1:p.Ile188Thr
XM_024450186.1:c.635T>C	XP_024305954.1:p.Ile212Thr
XM_024450187.1:c.635T>C	XP_024305955.1:p.Ile212Thr
XR_001751864.2:n.1677T>C
XR_001751865.1:n.1624T>C
XR_933240.3:n.1867T>C
NM_001127214.4:c.1430T>C	NP_001120686.1:p.Ile477Thr
NM_001243279.3:c.1430T>C MANE Select	NP_001230208.1:p.Ile477Thr
NM_001284316.2:c.635T>C	NP_001271245.1:p.Ile212Thr
NM_174917.5:c.1430T>C	NP_777577.2:p.Ile477Thr
NR_104293.2:n.1821T>C
NR_147928.2:n.1865T>C
NR_147929.2:n.1619T>C