Canonical Allele Identifier: CA1573470757

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840272_112840273delinsGA , CM000667.2:g.112840272_112840273delinsGA	GRCh38
NC_000005.9:g.112175969_112175970delinsGA , CM000667.1:g.112175969_112175970delinsGA	GRCh37
NC_000005.8:g.112203868_112203869delinsGA	NCBI36
NG_008481.4:g.152752_152753delinsGA , LRG_130:g.152752_152753delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4732_4733delinsGA	ENSP00000473355.2:p.Glu1578=
ENST00000505350.2:c.*4684_*4685delinsGA	ENSP00000481752.1:n.*4684_*4685delinsGA
ENST00000507379.6:c.4624_4625delinsGA	ENSP00000423224.2:p.Glu1542=
ENST00000509732.6:c.4678_4679delinsGA	ENSP00000426541.2:p.Glu1560=
ENST00000512211.7:c.4678_4679delinsGA	ENSP00000423828.3:p.Glu1560=
ENST00000257430.9:c.4678_4679delinsGA MANE Select	ENSP00000257430.4:p.Glu1560=
ENST00000257430.8:c.4678_4679delinsGA	ENSP00000257430.4:p.Glu1560=
ENST00000508376.6:c.4678_4679delinsGA	ENSP00000427089.2:p.Glu1560=
ENST00000508624.5:c.*4000_*4001delinsGA	ENSP00000424265.1:n.*4000_*4001delinsGA
ENST00000520401.1:c.230+11300_230+11301delinsGA
NM_000038.5:c.4678_4679delinsGA	NP_000029.2:p.Glu1560=
NM_001127510.2:c.4678_4679delinsGA	NP_001120982.1:p.Glu1560=
NM_001127511.2:c.4624_4625delinsGA	NP_001120983.2:p.Glu1542=
NM_001354895.1:c.4678_4679delinsGA	NP_001341824.1:p.Glu1560=
NM_001354896.1:c.4732_4733delinsGA	NP_001341825.1:p.Glu1578=
NM_001354897.1:c.4708_4709delinsGA	NP_001341826.1:p.Glu1570=
NM_001354898.1:c.4603_4604delinsGA	NP_001341827.1:p.Glu1535=
NM_001354899.1:c.4594_4595delinsGA	NP_001341828.1:p.Glu1532=
NM_001354900.1:c.4555_4556delinsGA	NP_001341829.1:p.Glu1519=
NM_001354901.1:c.4501_4502delinsGA	NP_001341830.1:p.Glu1501=
NM_001354902.1:c.4405_4406delinsGA	NP_001341831.1:p.Glu1469=
NM_001354903.1:c.4375_4376delinsGA	NP_001341832.1:p.Glu1459=
NM_001354904.1:c.4300_4301delinsGA	NP_001341833.1:p.Glu1434=
NM_001354905.1:c.4198_4199delinsGA	NP_001341834.1:p.Glu1400=
NM_001354906.1:c.3829_3830delinsGA	NP_001341835.1:p.Glu1277=
NM_000038.6:c.4678_4679delinsGA MANE Select	NP_000029.2:p.Glu1560=
NM_001127510.3:c.4678_4679delinsGA	NP_001120982.1:p.Glu1560=
NM_001127511.3:c.4624_4625delinsGA	NP_001120983.2:p.Glu1542=
NM_001354895.2:c.4678_4679delinsGA	NP_001341824.1:p.Glu1560=
NM_001354896.2:c.4732_4733delinsGA	NP_001341825.1:p.Glu1578=
NM_001354897.2:c.4708_4709delinsGA	NP_001341826.1:p.Glu1570=
NM_001354898.2:c.4603_4604delinsGA	NP_001341827.1:p.Glu1535=
NM_001354899.2:c.4594_4595delinsGA	NP_001341828.1:p.Glu1532=
NM_001354900.2:c.4555_4556delinsGA	NP_001341829.1:p.Glu1519=
NM_001354901.2:c.4501_4502delinsGA	NP_001341830.1:p.Glu1501=
NM_001354902.2:c.4405_4406delinsGA	NP_001341831.1:p.Glu1469=
NM_001354903.2:c.4375_4376delinsGA	NP_001341832.1:p.Glu1459=
NM_001354904.2:c.4300_4301delinsGA	NP_001341833.1:p.Glu1434=
NM_001354905.2:c.4198_4199delinsGA	NP_001341834.1:p.Glu1400=
NM_001354906.2:c.3829_3830delinsGA	NP_001341835.1:p.Glu1277=