Canonical Allele Identifier: CA1573508643

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828878_112828879delinsAT , CM000667.2:g.112828878_112828879delinsAT	GRCh38
NC_000005.9:g.112164575_112164576delinsAT , CM000667.1:g.112164575_112164576delinsAT	GRCh37
NC_000005.8:g.112192474_112192475delinsAT	NCBI36
NG_008481.4:g.141358_141359delinsAT , LRG_130:g.141358_141359delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1409-6073_1409-6072delinsAT	ENSP00000484935.2:n.1409-6073_1409-6072de...
ENST00000504915.3:c.1703_1704delinsAT	ENSP00000473355.2:p.Asn568=
ENST00000505084.2:n.1705_1706delinsAT
ENST00000505350.2:c.*1655_*1656delinsAT	ENSP00000481752.1:n.*1655_*1656delinsAT
ENST00000507379.6:c.1595_1596delinsAT	ENSP00000423224.2:p.Asn532=
ENST00000509732.6:c.1649_1650delinsAT	ENSP00000426541.2:p.Asn550=
ENST00000512211.7:c.1649_1650delinsAT	ENSP00000423828.3:p.Asn550=
ENST00000257430.9:c.1649_1650delinsAT MANE Select	ENSP00000257430.4:p.Asn550=
ENST00000257430.8:c.1649_1650delinsAT	ENSP00000257430.4:p.Asn550=
ENST00000502371.2:c.97-6073_97-6072delinsAT
ENST00000504915.2:c.338_339delinsAT	ENSP00000473355.1:p.Asn113=
ENST00000505084.1:n.136_137delinsAT
ENST00000507379.5:c.1595_1596delinsAT	ENSP00000423224.1:p.Asn532=
ENST00000508376.6:c.1649_1650delinsAT	ENSP00000427089.2:p.Asn550=
ENST00000508624.5:c.*971_*972delinsAT	ENSP00000424265.1:n.*971_*972delinsAT
ENST00000512211.6:c.1649_1650delinsAT	ENSP00000423828.2:p.Asn550=
ENST00000520401.1:c.136_137delinsAT
NM_000038.5:c.1649_1650delinsAT	NP_000029.2:p.Asn550=
NM_001127510.2:c.1649_1650delinsAT	NP_001120982.1:p.Asn550=
NM_001127511.2:c.1595_1596delinsAT	NP_001120983.2:p.Asn532=
NM_001354895.1:c.1649_1650delinsAT	NP_001341824.1:p.Asn550=
NM_001354896.1:c.1703_1704delinsAT	NP_001341825.1:p.Asn568=
NM_001354897.1:c.1679_1680delinsAT	NP_001341826.1:p.Asn560=
NM_001354898.1:c.1574_1575delinsAT	NP_001341827.1:p.Asn525=
NM_001354899.1:c.1565_1566delinsAT	NP_001341828.1:p.Asn522=
NM_001354900.1:c.1526_1527delinsAT	NP_001341829.1:p.Asn509=
NM_001354901.1:c.1472_1473delinsAT	NP_001341830.1:p.Asn491=
NM_001354902.1:c.1376_1377delinsAT	NP_001341831.1:p.Asn459=
NM_001354903.1:c.1346_1347delinsAT	NP_001341832.1:p.Asn449=
NM_001354904.1:c.1271_1272delinsAT	NP_001341833.1:p.Asn424=
NM_001354905.1:c.1169_1170delinsAT	NP_001341834.1:p.Asn390=
NM_001354906.1:c.800_801delinsAT	NP_001341835.1:p.Asn267=
NM_000038.6:c.1649_1650delinsAT MANE Select	NP_000029.2:p.Asn550=
NM_001127510.3:c.1649_1650delinsAT	NP_001120982.1:p.Asn550=
NM_001127511.3:c.1595_1596delinsAT	NP_001120983.2:p.Asn532=
NM_001354895.2:c.1649_1650delinsAT	NP_001341824.1:p.Asn550=
NM_001354896.2:c.1703_1704delinsAT	NP_001341825.1:p.Asn568=
NM_001354897.2:c.1679_1680delinsAT	NP_001341826.1:p.Asn560=
NM_001354898.2:c.1574_1575delinsAT	NP_001341827.1:p.Asn525=
NM_001354899.2:c.1565_1566delinsAT	NP_001341828.1:p.Asn522=
NM_001354900.2:c.1526_1527delinsAT	NP_001341829.1:p.Asn509=
NM_001354901.2:c.1472_1473delinsAT	NP_001341830.1:p.Asn491=
NM_001354902.2:c.1376_1377delinsAT	NP_001341831.1:p.Asn459=
NM_001354903.2:c.1346_1347delinsAT	NP_001341832.1:p.Asn449=
NM_001354904.2:c.1271_1272delinsAT	NP_001341833.1:p.Asn424=
NM_001354905.2:c.1169_1170delinsAT	NP_001341834.1:p.Asn390=
NM_001354906.2:c.800_801delinsAT	NP_001341835.1:p.Asn267=