Canonical Allele Identifier: CA2634928030

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89153636-G-GAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89153636_89153637insAT , CM000678.2:g.89153636_89153637insAT	GRCh38
NC_000016.9:g.89220044_89220045insAT , CM000678.1:g.89220044_89220045insAT	GRCh37
NC_000016.8:g.87747545_87747546insAT	NCBI36
NG_031961.1:g.64828_64829insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1614-454_1614-453insAT	ENSP00000320646.4:n.1614-454_1614-453insAT
ENST00000614302.5:c.1614-454_1614-453insAT MANE Select	ENSP00000479130.1:n.1614-454_1614-453insAT
ENST00000649953.1:c.1824-454_1824-453insAT	ENSP00000497456.1:n.1824-454_1824-453insAT
ENST00000317447.8:c.1614-454_1614-453insAT	ENSP00000320646.4:n.1614-454_1614-453insAT
ENST00000378345.8:c.819-454_819-453insAT	ENSP00000367596.4:n.819-454_819-453insAT
ENST00000393145.5:n.6070_6071insAT
ENST00000406948.7:c.1614-454_1614-453insAT	ENSP00000384627.3:n.1614-454_1614-453insAT
ENST00000537116.5:n.740-454_740-453insAT
ENST00000537155.1:n.354-454_354-453insAT
ENST00000542688.5:c.*358-454_*358-453insAT	ENSP00000446281.1:n.*358-454_*358-453insAT
ENST00000614302.4:c.1614-454_1614-453insAT	ENSP00000479130.1:n.1614-454_1614-453insAT
NM_001127214.3:c.1614-454_1614-453insAT	NP_001120686.1:n.1614-454_1614-453insAT
NM_001243279.2:c.1614-454_1614-453insAT	NP_001230208.1:n.1614-454_1614-453insAT
NM_001284316.1:c.819-454_819-453insAT	NP_001271245.1:n.819-454_819-453insAT
NM_174917.4:c.1614-454_1614-453insAT	NP_777577.2:n.1614-454_1614-453insAT
NR_045667.2:n.740-454_740-453insAT
NR_104293.1:n.2048-454_2048-453insAT
XR_933239.1:n.2055-454_2055-453insAT
XR_933240.1:n.2052-454_2052-453insAT
XR_933241.1:n.1809-454_1809-453insAT
NR_147928.1:n.2092-454_2092-453insAT
NR_147929.1:n.1846-454_1846-453insAT
XM_017023020.2:c.-3491-454_-3491-453insAT	XP_016878509.1:n.-3491-454_-3491-453insAT
XM_024450187.1:c.819-454_819-453insAT	XP_024305955.1:n.819-454_819-453insAT
XR_001751864.2:n.1861-454_1861-453insAT
XR_933240.3:n.2051-454_2051-453insAT
NM_001127214.4:c.1614-454_1614-453insAT	NP_001120686.1:n.1614-454_1614-453insAT
NM_001243279.3:c.1614-454_1614-453insAT MANE Select	NP_001230208.1:n.1614-454_1614-453insAT
NM_001284316.2:c.819-454_819-453insAT	NP_001271245.1:n.819-454_819-453insAT
NM_174917.5:c.1614-454_1614-453insAT	NP_777577.2:n.1614-454_1614-453insAT
NR_104293.2:n.2005-454_2005-453insAT
NR_147928.2:n.2049-454_2049-453insAT
NR_147929.2:n.1803-454_1803-453insAT