Canonical Allele Identifier: CA1573472636

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840544_112840546delinsCTT , CM000667.2:g.112840544_112840546delinsCTT	GRCh38
NC_000005.9:g.112176241_112176243delinsCTT , CM000667.1:g.112176241_112176243delinsCTT	GRCh37
NC_000005.8:g.112204140_112204142delinsCTT	NCBI36
NG_008481.4:g.153024_153026delinsCTT , LRG_130:g.153024_153026delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5004_5006delinsCTT	ENSP00000473355.2:p.Asn1668=
ENST00000505350.2:c.*4956_*4958delinsCTT	ENSP00000481752.1:n.*4956_*4958delinsCTT
ENST00000507379.6:c.4896_4898delinsCTT	ENSP00000423224.2:p.Asn1632=
ENST00000509732.6:c.4950_4952delinsCTT	ENSP00000426541.2:p.Asn1650=
ENST00000512211.7:c.4950_4952delinsCTT	ENSP00000423828.3:p.Asn1650=
ENST00000257430.9:c.4950_4952delinsCTT MANE Select	ENSP00000257430.4:p.Asn1650=
ENST00000257430.8:c.4950_4952delinsCTT	ENSP00000257430.4:p.Asn1650=
ENST00000508376.6:c.4950_4952delinsCTT	ENSP00000427089.2:p.Asn1650=
ENST00000508624.5:c.*4272_*4274delinsCTT	ENSP00000424265.1:n.*4272_*4274delinsCTT
ENST00000520401.1:c.230+11572_230+11574delinsCTT
NM_000038.5:c.4950_4952delinsCTT	NP_000029.2:p.Asn1650=
NM_001127510.2:c.4950_4952delinsCTT	NP_001120982.1:p.Asn1650=
NM_001127511.2:c.4896_4898delinsCTT	NP_001120983.2:p.Asn1632=
NM_001354895.1:c.4950_4952delinsCTT	NP_001341824.1:p.Asn1650=
NM_001354896.1:c.5004_5006delinsCTT	NP_001341825.1:p.Asn1668=
NM_001354897.1:c.4980_4982delinsCTT	NP_001341826.1:p.Asn1660=
NM_001354898.1:c.4875_4877delinsCTT	NP_001341827.1:p.Asn1625=
NM_001354899.1:c.4866_4868delinsCTT	NP_001341828.1:p.Asn1622=
NM_001354900.1:c.4827_4829delinsCTT	NP_001341829.1:p.Asn1609=
NM_001354901.1:c.4773_4775delinsCTT	NP_001341830.1:p.Asn1591=
NM_001354902.1:c.4677_4679delinsCTT	NP_001341831.1:p.Asn1559=
NM_001354903.1:c.4647_4649delinsCTT	NP_001341832.1:p.Asn1549=
NM_001354904.1:c.4572_4574delinsCTT	NP_001341833.1:p.Asn1524=
NM_001354905.1:c.4470_4472delinsCTT	NP_001341834.1:p.Asn1490=
NM_001354906.1:c.4101_4103delinsCTT	NP_001341835.1:p.Asn1367=
NM_000038.6:c.4950_4952delinsCTT MANE Select	NP_000029.2:p.Asn1650=
NM_001127510.3:c.4950_4952delinsCTT	NP_001120982.1:p.Asn1650=
NM_001127511.3:c.4896_4898delinsCTT	NP_001120983.2:p.Asn1632=
NM_001354895.2:c.4950_4952delinsCTT	NP_001341824.1:p.Asn1650=
NM_001354896.2:c.5004_5006delinsCTT	NP_001341825.1:p.Asn1668=
NM_001354897.2:c.4980_4982delinsCTT	NP_001341826.1:p.Asn1660=
NM_001354898.2:c.4875_4877delinsCTT	NP_001341827.1:p.Asn1625=
NM_001354899.2:c.4866_4868delinsCTT	NP_001341828.1:p.Asn1622=
NM_001354900.2:c.4827_4829delinsCTT	NP_001341829.1:p.Asn1609=
NM_001354901.2:c.4773_4775delinsCTT	NP_001341830.1:p.Asn1591=
NM_001354902.2:c.4677_4679delinsCTT	NP_001341831.1:p.Asn1559=
NM_001354903.2:c.4647_4649delinsCTT	NP_001341832.1:p.Asn1549=
NM_001354904.2:c.4572_4574delinsCTT	NP_001341833.1:p.Asn1524=
NM_001354905.2:c.4470_4472delinsCTT	NP_001341834.1:p.Asn1490=
NM_001354906.2:c.4101_4103delinsCTT	NP_001341835.1:p.Asn1367=