Canonical Allele Identifier: CA2241515439

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145387_89145388delinsAC , CM000678.2:g.89145387_89145388delinsAC	GRCh38
NC_000016.9:g.89211795_89211796delinsAC , CM000678.1:g.89211795_89211796delinsAC	GRCh37
NC_000016.8:g.87739296_87739297delinsAC	NCBI36
NG_031961.1:g.56579_56580delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1487_1488delinsAC	ENSP00000320646.4:p.His496=
ENST00000614302.5:c.1487_1488delinsAC MANE Select	ENSP00000479130.1:p.His496=
ENST00000649953.1:c.1697_1698delinsAC	ENSP00000497456.1:p.His566=
ENST00000317447.8:c.1487_1488delinsAC	ENSP00000320646.4:p.His496=
ENST00000378345.8:c.692_693delinsAC	ENSP00000367596.4:p.His231=
ENST00000406948.7:c.1487_1488delinsAC	ENSP00000384627.3:p.His496=
ENST00000537116.5:n.613_614delinsAC
ENST00000537155.1:n.227_228delinsAC
ENST00000542688.5:c.*231_*232delinsAC	ENSP00000446281.1:n.*231_*232delinsAC
ENST00000544543.5:c.692_693delinsAC	ENSP00000442781.1:p.His231=
ENST00000562204.1:n.460_461delinsAC
ENST00000614302.4:c.1487_1488delinsAC	ENSP00000479130.1:p.His496=
NM_001127214.3:c.1487_1488delinsAC	NP_001120686.1:p.His496=
NM_001243279.2:c.1487_1488delinsAC	NP_001230208.1:p.His496=
NM_001284316.1:c.692_693delinsAC	NP_001271245.1:p.His231=
NM_174917.4:c.1487_1488delinsAC	NP_777577.2:p.His496=
NR_045667.2:n.613_614delinsAC
NR_104293.1:n.1921_1922delinsAC
XM_005256293.1:c.1487_1488delinsAC	XP_005256350.1:p.His496=
XM_011522942.1:c.1487_1488delinsAC	XP_011521244.1:p.His496=
XM_011522943.1:c.1487_1488delinsAC	XP_011521245.1:p.His496=
XR_933239.1:n.1928_1929delinsAC
XR_933240.1:n.1925_1926delinsAC
XR_933241.1:n.1682_1683delinsAC
NR_147928.1:n.1965_1966delinsAC
NR_147929.1:n.1719_1720delinsAC
XM_005256293.2:c.1487_1488delinsAC	XP_005256350.1:p.His496=
XM_017023018.1:c.1487_1488delinsAC	XP_016878507.1:p.His496=
XM_017023019.1:c.1487_1488delinsAC	XP_016878508.1:p.His496=
XM_017023020.2:c.-3618_-3617delinsAC	XP_016878509.1:n.-3618_-3617delinsAC
XM_017023022.1:c.620_621delinsAC	XP_016878511.1:p.His207=
XM_024450186.1:c.692_693delinsAC	XP_024305954.1:p.His231=
XM_024450187.1:c.692_693delinsAC	XP_024305955.1:p.His231=
XR_001751864.2:n.1734_1735delinsAC
XR_001751865.1:n.1681_1682delinsAC
XR_933240.3:n.1924_1925delinsAC
NM_001127214.4:c.1487_1488delinsAC	NP_001120686.1:p.His496=
NM_001243279.3:c.1487_1488delinsAC MANE Select	NP_001230208.1:p.His496=
NM_001284316.2:c.692_693delinsAC	NP_001271245.1:p.His231=
NM_174917.5:c.1487_1488delinsAC	NP_777577.2:p.His496=
NR_104293.2:n.1878_1879delinsAC
NR_147928.2:n.1922_1923delinsAC
NR_147929.2:n.1676_1677delinsAC