Canonical Allele Identifier: CA497148434

Gene: ACSF3

Linked Data

• MyVariant Identifiers: chr16:g.89220522G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154114G>T , CM000678.2:g.89154114G>T	GRCh38
NC_000016.9:g.89220522G>T , CM000678.1:g.89220522G>T	GRCh37
NC_000016.8:g.87748023G>T	NCBI36
NG_031961.1:g.65306G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1638G>T	ENSP00000320646.4:p.Val546=
ENST00000614302.5:c.1638G>T MANE Select	ENSP00000479130.1:p.Val546=
ENST00000649953.1:c.1848G>T	ENSP00000497456.1:p.Val616=
ENST00000317447.8:c.1638G>T	ENSP00000320646.4:p.Val546=
ENST00000378345.8:c.843G>T	ENSP00000367596.4:p.Val281=
ENST00000393145.5:n.6548G>T
ENST00000406948.7:c.1638G>T	ENSP00000384627.3:p.Val546=
ENST00000537116.5:n.764G>T
ENST00000537155.1:n.378G>T
ENST00000542688.5:c.*382G>T	ENSP00000446281.1:n.*382G>T
ENST00000614302.4:c.1638G>T	ENSP00000479130.1:p.Val546=
NM_001127214.3:c.1638G>T	NP_001120686.1:p.Val546=
NM_001243279.2:c.1638G>T	NP_001230208.1:p.Val546=
NM_001284316.1:c.843G>T	NP_001271245.1:p.Val281=
NM_174917.4:c.1638G>T	NP_777577.2:p.Val546=
NR_045667.2:n.764G>T
NR_104293.1:n.2072G>T
XR_933239.1:n.2079G>T
XR_933240.1:n.2076G>T
XR_933241.1:n.1833G>T
NR_147928.1:n.2116G>T
NR_147929.1:n.1870G>T
XM_017023020.2:c.-3467G>T	XP_016878509.1:n.-3467G>T
XM_024450187.1:c.843G>T	XP_024305955.1:p.Val281=
XR_001751864.2:n.1885G>T
XR_933240.3:n.2075G>T
NM_001127214.4:c.1638G>T	NP_001120686.1:p.Val546=
NM_001243279.3:c.1638G>T MANE Select	NP_001230208.1:p.Val546=
NM_001284316.2:c.843G>T	NP_001271245.1:p.Val281=
NM_174917.5:c.1638G>T	NP_777577.2:p.Val546=
NR_104293.2:n.2029G>T
NR_147928.2:n.2073G>T
NR_147929.2:n.1827G>T