Canonical Allele Identifier: CA2241515782

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145958C= , CM000678.2:g.89145958C=	GRCh38
NC_000016.9:g.89212366C= , CM000678.1:g.89212366C=	GRCh37
NC_000016.8:g.87739867C=	NCBI36
NG_031961.1:g.57150C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000317447.9:c.1522C=	ENSP00000320646.4:p.Pro508=
ENST00000614302.5:c.1522C= MANE Select	ENSP00000479130.1:p.Pro508=
ENST00000649953.1:c.1732C=	ENSP00000497456.1:p.Pro578=
ENST00000317447.8:c.1522C=	ENSP00000320646.4:p.Pro508=
ENST00000378345.8:c.727C=	ENSP00000367596.4:p.Pro243=
ENST00000406948.7:c.1522C=	ENSP00000384627.3:p.Pro508=
ENST00000535176.1:c.9C=
ENST00000537116.5:n.648C=
ENST00000537155.1:n.262C=
ENST00000542688.5:c.*266C=	ENSP00000446281.1:n.*266C=
ENST00000562204.1:n.495C=
ENST00000614302.4:c.1522C=	ENSP00000479130.1:p.Pro508=
NM_001127214.3:c.1522C=	NP_001120686.1:p.Pro508=
NM_001243279.2:c.1522C=	NP_001230208.1:p.Pro508=
NM_001284316.1:c.727C=	NP_001271245.1:p.Pro243=
NM_174917.4:c.1522C=	NP_777577.2:p.Pro508=
NR_045667.2:n.648C=
NR_104293.1:n.1956C=
XM_005256293.1:c.1522C=	XP_005256350.1:p.Pro508=
XM_011522942.1:c.1522C=	XP_011521244.1:p.Pro508=
XM_011522943.1:c.1522C=	XP_011521245.1:p.Pro508=
XR_933239.1:n.1963C=
XR_933240.1:n.1960C=
XR_933241.1:n.1717C=
NR_147928.1:n.2000C=
NR_147929.1:n.1754C=
XM_005256293.2:c.1522C=	XP_005256350.1:p.Pro508=
XM_017023018.1:c.1522C=	XP_016878507.1:p.Pro508=
XM_017023019.1:c.1522C=	XP_016878508.1:p.Pro508=
XM_017023020.2:c.-3583C=	XP_016878509.1:n.-3583C=
XM_017023022.1:c.655C=	XP_016878511.1:p.Pro219=
XM_024450186.1:c.727C=	XP_024305954.1:p.Pro243=
XM_024450187.1:c.727C=	XP_024305955.1:p.Pro243=
XR_001751864.2:n.1769C=
XR_001751865.1:n.1716C=
XR_933240.3:n.1959C=
NM_001127214.4:c.1522C=	NP_001120686.1:p.Pro508=
NM_001243279.3:c.1522C= MANE Select	NP_001230208.1:p.Pro508=
NM_001284316.2:c.727C=	NP_001271245.1:p.Pro243=
NM_174917.5:c.1522C=	NP_777577.2:p.Pro508=
NR_104293.2:n.1913C=
NR_147928.2:n.1957C=
NR_147929.2:n.1711C=