Canonical Allele Identifier: CA497148499

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89154168-T-C
• MyVariant Identifiers: chr16:g.89220576T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154168T>C , CM000678.2:g.89154168T>C	GRCh38
NC_000016.9:g.89220576T>C , CM000678.1:g.89220576T>C	GRCh37
NC_000016.8:g.87748077T>C	NCBI36
NG_031961.1:g.65360T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1692T>C	ENSP00000320646.4:p.Ile564=
ENST00000614302.5:c.1692T>C MANE Select	ENSP00000479130.1:p.Ile564=
ENST00000649953.1:c.1902T>C	ENSP00000497456.1:p.Ile634=
ENST00000317447.8:c.1692T>C	ENSP00000320646.4:p.Ile564=
ENST00000378345.8:c.897T>C	ENSP00000367596.4:p.Ile299=
ENST00000393145.5:n.6602T>C
ENST00000406948.7:c.1692T>C	ENSP00000384627.3:p.Ile564=
ENST00000537116.5:n.818T>C
ENST00000537155.1:n.432T>C
ENST00000542688.5:c.*436T>C	ENSP00000446281.1:n.*436T>C
ENST00000614302.4:c.1692T>C	ENSP00000479130.1:p.Ile564=
NM_001127214.3:c.1692T>C	NP_001120686.1:p.Ile564=
NM_001243279.2:c.1692T>C	NP_001230208.1:p.Ile564=
NM_001284316.1:c.897T>C	NP_001271245.1:p.Ile299=
NM_174917.4:c.1692T>C	NP_777577.2:p.Ile564=
NR_045667.2:n.818T>C
NR_104293.1:n.2126T>C
XR_933239.1:n.2133T>C
XR_933240.1:n.2130T>C
XR_933241.1:n.1887T>C
NR_147928.1:n.2170T>C
NR_147929.1:n.1924T>C
XM_017023020.2:c.-3413T>C	XP_016878509.1:n.-3413T>C
XM_024450187.1:c.897T>C	XP_024305955.1:p.Ile299=
XR_001751864.2:n.1939T>C
XR_933240.3:n.2129T>C
NM_001127214.4:c.1692T>C	NP_001120686.1:p.Ile564=
NM_001243279.3:c.1692T>C MANE Select	NP_001230208.1:p.Ile564=
NM_001284316.2:c.897T>C	NP_001271245.1:p.Ile299=
NM_174917.5:c.1692T>C	NP_777577.2:p.Ile564=
NR_104293.2:n.2083T>C
NR_147928.2:n.2127T>C
NR_147929.2:n.1881T>C