Canonical Allele Identifier: CA1573470337

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840232_112840248delinsTGAAAACCAAGAGAAAG , CM000667.2:g.112840232_112840248delinsTGAAAACCAAGAGAAAG	GRCh38
NC_000005.9:g.112175929_112175945delinsTGAAAACCAAGAGAAAG , CM000667.1:g.112175929_112175945delinsTGAAAACCAAGAGAAAG	GRCh37
NC_000005.8:g.112203828_112203844delinsTGAAAACCAAGAGAAAG	NCBI36
NG_008481.4:g.152712_152728delinsTGAAAACCAAGAGAAAG , LRG_130:g.152712_152728delinsTGAAAACCAAGAGAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4692_4708delinsTGAAAACCAAGAGAAAG	ENSP00000473355.2:p.Asn1564=
ENST00000505350.2:c.*4644_*4660delinsTGAAAACCAAGAGAAAG	ENSP00000481752.1:n.*4644_*4660delinsTGAAAACCAAGAGAAAG
ENST00000507379.6:c.4584_4600delinsTGAAAACCAAGAGAAAG	ENSP00000423224.2:p.Asn1528=
ENST00000509732.6:c.4638_4654delinsTGAAAACCAAGAGAAAG	ENSP00000426541.2:p.Asn1546=
ENST00000512211.7:c.4638_4654delinsTGAAAACCAAGAGAAAG	ENSP00000423828.3:p.Asn1546=
ENST00000257430.9:c.4638_4654delinsTGAAAACCAAGAGAAAG MANE Select	ENSP00000257430.4:p.Asn1546=
ENST00000257430.8:c.4638_4654delinsTGAAAACCAAGAGAAAG	ENSP00000257430.4:p.Asn1546=
ENST00000508376.6:c.4638_4654delinsTGAAAACCAAGAGAAAG	ENSP00000427089.2:p.Asn1546=
ENST00000508624.5:c.*3960_*3976delinsTGAAAACCAAGAGAAAG	ENSP00000424265.1:n.*3960_*3976delinsTGAAAACCAAGAGAAAG
ENST00000520401.1:c.230+11260_230+11276delinsTGAAAACCAAGAGAAAG
NM_000038.5:c.4638_4654delinsTGAAAACCAAGAGAAAG	NP_000029.2:p.Asn1546=
NM_001127510.2:c.4638_4654delinsTGAAAACCAAGAGAAAG	NP_001120982.1:p.Asn1546=
NM_001127511.2:c.4584_4600delinsTGAAAACCAAGAGAAAG	NP_001120983.2:p.Asn1528=
NM_001354895.1:c.4638_4654delinsTGAAAACCAAGAGAAAG	NP_001341824.1:p.Asn1546=
NM_001354896.1:c.4692_4708delinsTGAAAACCAAGAGAAAG	NP_001341825.1:p.Asn1564=
NM_001354897.1:c.4668_4684delinsTGAAAACCAAGAGAAAG	NP_001341826.1:p.Asn1556=
NM_001354898.1:c.4563_4579delinsTGAAAACCAAGAGAAAG	NP_001341827.1:p.Asn1521=
NM_001354899.1:c.4554_4570delinsTGAAAACCAAGAGAAAG	NP_001341828.1:p.Asn1518=
NM_001354900.1:c.4515_4531delinsTGAAAACCAAGAGAAAG	NP_001341829.1:p.Asn1505=
NM_001354901.1:c.4461_4477delinsTGAAAACCAAGAGAAAG	NP_001341830.1:p.Asn1487=
NM_001354902.1:c.4365_4381delinsTGAAAACCAAGAGAAAG	NP_001341831.1:p.Asn1455=
NM_001354903.1:c.4335_4351delinsTGAAAACCAAGAGAAAG	NP_001341832.1:p.Asn1445=
NM_001354904.1:c.4260_4276delinsTGAAAACCAAGAGAAAG	NP_001341833.1:p.Asn1420=
NM_001354905.1:c.4158_4174delinsTGAAAACCAAGAGAAAG	NP_001341834.1:p.Asn1386=
NM_001354906.1:c.3789_3805delinsTGAAAACCAAGAGAAAG	NP_001341835.1:p.Asn1263=
NM_000038.6:c.4638_4654delinsTGAAAACCAAGAGAAAG MANE Select	NP_000029.2:p.Asn1546=
NM_001127510.3:c.4638_4654delinsTGAAAACCAAGAGAAAG	NP_001120982.1:p.Asn1546=
NM_001127511.3:c.4584_4600delinsTGAAAACCAAGAGAAAG	NP_001120983.2:p.Asn1528=
NM_001354895.2:c.4638_4654delinsTGAAAACCAAGAGAAAG	NP_001341824.1:p.Asn1546=
NM_001354896.2:c.4692_4708delinsTGAAAACCAAGAGAAAG	NP_001341825.1:p.Asn1564=
NM_001354897.2:c.4668_4684delinsTGAAAACCAAGAGAAAG	NP_001341826.1:p.Asn1556=
NM_001354898.2:c.4563_4579delinsTGAAAACCAAGAGAAAG	NP_001341827.1:p.Asn1521=
NM_001354899.2:c.4554_4570delinsTGAAAACCAAGAGAAAG	NP_001341828.1:p.Asn1518=
NM_001354900.2:c.4515_4531delinsTGAAAACCAAGAGAAAG	NP_001341829.1:p.Asn1505=
NM_001354901.2:c.4461_4477delinsTGAAAACCAAGAGAAAG	NP_001341830.1:p.Asn1487=
NM_001354902.2:c.4365_4381delinsTGAAAACCAAGAGAAAG	NP_001341831.1:p.Asn1455=
NM_001354903.2:c.4335_4351delinsTGAAAACCAAGAGAAAG	NP_001341832.1:p.Asn1445=
NM_001354904.2:c.4260_4276delinsTGAAAACCAAGAGAAAG	NP_001341833.1:p.Asn1420=
NM_001354905.2:c.4158_4174delinsTGAAAACCAAGAGAAAG	NP_001341834.1:p.Asn1386=
NM_001354906.2:c.3789_3805delinsTGAAAACCAAGAGAAAG	NP_001341835.1:p.Asn1263=