Canonical Allele Identifier: CA397150941

Gene: ACSF3

Linked Data

• MyVariant Identifiers: chr16:g.89220604C>G (hg19) ; chr16:g.89154196C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154196C>G , CM000678.2:g.89154196C>G	GRCh38
NC_000016.9:g.89220604C>G , CM000678.1:g.89220604C>G	GRCh37
NC_000016.8:g.87748105C>G	NCBI36
NG_031961.1:g.65388C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1720C>G	ENSP00000320646.4:p.His574Asp
ENST00000614302.5:c.1720C>G MANE Select	ENSP00000479130.1:p.His574Asp
ENST00000649953.1:c.1930C>G	ENSP00000497456.1:p.His644Asp
ENST00000317447.8:c.1720C>G	ENSP00000320646.4:p.His574Asp
ENST00000378345.8:c.925C>G	ENSP00000367596.4:p.His309Asp
ENST00000393145.5:n.6630C>G
ENST00000406948.7:c.1720C>G	ENSP00000384627.3:p.His574Asp
ENST00000537116.5:n.846C>G
ENST00000537155.1:n.460C>G
ENST00000542688.5:c.*464C>G	ENSP00000446281.1:n.*464C>G
ENST00000614302.4:c.1720C>G	ENSP00000479130.1:p.His574Asp
NM_001127214.3:c.1720C>G	NP_001120686.1:p.His574Asp
NM_001243279.2:c.1720C>G	NP_001230208.1:p.His574Asp
NM_001284316.1:c.925C>G	NP_001271245.1:p.His309Asp
NM_174917.4:c.1720C>G	NP_777577.2:p.His574Asp
NR_045667.2:n.846C>G
NR_104293.1:n.2154C>G
XR_933239.1:n.2161C>G
XR_933240.1:n.2158C>G
XR_933241.1:n.1915C>G
NR_147928.1:n.2198C>G
NR_147929.1:n.1952C>G
XM_017023020.2:c.-3385C>G	XP_016878509.1:n.-3385C>G
XM_024450187.1:c.925C>G	XP_024305955.1:p.His309Asp
XR_001751864.2:n.1967C>G
XR_933240.3:n.2157C>G
NM_001127214.4:c.1720C>G	NP_001120686.1:p.His574Asp
NM_001243279.3:c.1720C>G MANE Select	NP_001230208.1:p.His574Asp
NM_001284316.2:c.925C>G	NP_001271245.1:p.His309Asp
NM_174917.5:c.1720C>G	NP_777577.2:p.His574Asp
NR_104293.2:n.2111C>G
NR_147928.2:n.2155C>G
NR_147929.2:n.1909C>G