Canonical Allele Identifier: CA397150526

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89154134-T-C
• MyVariant Identifiers: chr16:g.89220542T>C (hg19) ; chr16:g.89154134T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154134T>C , CM000678.2:g.89154134T>C	GRCh38
NC_000016.9:g.89220542T>C , CM000678.1:g.89220542T>C	GRCh37
NC_000016.8:g.87748043T>C	NCBI36
NG_031961.1:g.65326T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1658T>C	ENSP00000320646.4:p.Val553Ala
ENST00000614302.5:c.1658T>C MANE Select	ENSP00000479130.1:p.Val553Ala
ENST00000649953.1:c.1868T>C	ENSP00000497456.1:p.Val623Ala
ENST00000317447.8:c.1658T>C	ENSP00000320646.4:p.Val553Ala
ENST00000378345.8:c.863T>C	ENSP00000367596.4:p.Val288Ala
ENST00000393145.5:n.6568T>C
ENST00000406948.7:c.1658T>C	ENSP00000384627.3:p.Val553Ala
ENST00000537116.5:n.784T>C
ENST00000537155.1:n.398T>C
ENST00000542688.5:c.*402T>C	ENSP00000446281.1:n.*402T>C
ENST00000614302.4:c.1658T>C	ENSP00000479130.1:p.Val553Ala
NM_001127214.3:c.1658T>C	NP_001120686.1:p.Val553Ala
NM_001243279.2:c.1658T>C	NP_001230208.1:p.Val553Ala
NM_001284316.1:c.863T>C	NP_001271245.1:p.Val288Ala
NM_174917.4:c.1658T>C	NP_777577.2:p.Val553Ala
NR_045667.2:n.784T>C
NR_104293.1:n.2092T>C
XR_933239.1:n.2099T>C
XR_933240.1:n.2096T>C
XR_933241.1:n.1853T>C
NR_147928.1:n.2136T>C
NR_147929.1:n.1890T>C
XM_017023020.2:c.-3447T>C	XP_016878509.1:n.-3447T>C
XM_024450187.1:c.863T>C	XP_024305955.1:p.Val288Ala
XR_001751864.2:n.1905T>C
XR_933240.3:n.2095T>C
NM_001127214.4:c.1658T>C	NP_001120686.1:p.Val553Ala
NM_001243279.3:c.1658T>C MANE Select	NP_001230208.1:p.Val553Ala
NM_001284316.2:c.863T>C	NP_001271245.1:p.Val288Ala
NM_174917.5:c.1658T>C	NP_777577.2:p.Val553Ala
NR_104293.2:n.2049T>C
NR_147928.2:n.2093T>C
NR_147929.2:n.1847T>C