Canonical Allele Identifier: CA397150820

Gene: ACSF3

Linked Data

• MyVariant Identifiers: chr16:g.89220583A>G (hg19) ; chr16:g.89154175A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154175A>G , CM000678.2:g.89154175A>G	GRCh38
NC_000016.9:g.89220583A>G , CM000678.1:g.89220583A>G	GRCh37
NC_000016.8:g.87748084A>G	NCBI36
NG_031961.1:g.65367A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1699A>G	ENSP00000320646.4:p.Lys567Glu
ENST00000614302.5:c.1699A>G MANE Select	ENSP00000479130.1:p.Lys567Glu
ENST00000649953.1:c.1909A>G	ENSP00000497456.1:p.Lys637Glu
ENST00000317447.8:c.1699A>G	ENSP00000320646.4:p.Lys567Glu
ENST00000378345.8:c.904A>G	ENSP00000367596.4:p.Lys302Glu
ENST00000393145.5:n.6609A>G
ENST00000406948.7:c.1699A>G	ENSP00000384627.3:p.Lys567Glu
ENST00000537116.5:n.825A>G
ENST00000537155.1:n.439A>G
ENST00000542688.5:c.*443A>G	ENSP00000446281.1:n.*443A>G
ENST00000614302.4:c.1699A>G	ENSP00000479130.1:p.Lys567Glu
NM_001127214.3:c.1699A>G	NP_001120686.1:p.Lys567Glu
NM_001243279.2:c.1699A>G	NP_001230208.1:p.Lys567Glu
NM_001284316.1:c.904A>G	NP_001271245.1:p.Lys302Glu
NM_174917.4:c.1699A>G	NP_777577.2:p.Lys567Glu
NR_045667.2:n.825A>G
NR_104293.1:n.2133A>G
XR_933239.1:n.2140A>G
XR_933240.1:n.2137A>G
XR_933241.1:n.1894A>G
NR_147928.1:n.2177A>G
NR_147929.1:n.1931A>G
XM_017023020.2:c.-3406A>G	XP_016878509.1:n.-3406A>G
XM_024450187.1:c.904A>G	XP_024305955.1:p.Lys302Glu
XR_001751864.2:n.1946A>G
XR_933240.3:n.2136A>G
NM_001127214.4:c.1699A>G	NP_001120686.1:p.Lys567Glu
NM_001243279.3:c.1699A>G MANE Select	NP_001230208.1:p.Lys567Glu
NM_001284316.2:c.904A>G	NP_001271245.1:p.Lys302Glu
NM_174917.5:c.1699A>G	NP_777577.2:p.Lys567Glu
NR_104293.2:n.2090A>G
NR_147928.2:n.2134A>G
NR_147929.2:n.1888A>G