Canonical Allele Identifier: CA1573484691

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112815530_112815537delinsTGTTTTGA , CM000667.2:g.112815530_112815537delinsTGTTTTGA	GRCh38
NC_000005.9:g.112151227_112151234delinsTGTTTTGA , CM000667.1:g.112151227_112151234delinsTGTTTTGA	GRCh37
NC_000005.8:g.112179126_112179133delinsTGTTTTGA	NCBI36
NG_008481.4:g.128010_128017delinsTGTTTTGA , LRG_130:g.128010_128017delinsTGTTTTGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.870_877delinsTGTTTTGA	ENSP00000484935.2:p.Ser290=
ENST00000504915.3:c.870_877delinsTGTTTTGA	ENSP00000473355.2:p.Ser290=
ENST00000505084.2:n.926_933delinsTGTTTTGA
ENST00000505350.2:c.*876_*883delinsTGTTTTGA	ENSP00000481752.1:n.*876_*883delinsTGTTTT...
ENST00000507379.6:c.816_823delinsTGTTTTGA	ENSP00000423224.2:p.Ser272=
ENST00000509732.6:c.870_877delinsTGTTTTGA	ENSP00000426541.2:p.Ser290=
ENST00000512211.7:c.870_877delinsTGTTTTGA	ENSP00000423828.3:p.Ser290=
ENST00000257430.9:c.870_877delinsTGTTTTGA MANE Select	ENSP00000257430.4:p.Ser290=
ENST00000257430.8:c.870_877delinsTGTTTTGA	ENSP00000257430.4:p.Ser290=
ENST00000507379.5:c.816_823delinsTGTTTTGA	ENSP00000423224.1:p.Ser272=
ENST00000508376.6:c.870_877delinsTGTTTTGA	ENSP00000427089.2:p.Ser290=
ENST00000508624.5:c.*192_*199delinsTGTTTTGA	ENSP00000424265.1:n.*192_*199delinsTGTTTT...
ENST00000512211.6:c.870_877delinsTGTTTTGA	ENSP00000423828.2:p.Ser290=
NM_000038.5:c.870_877delinsTGTTTTGA	NP_000029.2:p.Ser290=
NM_001127510.2:c.870_877delinsTGTTTTGA	NP_001120982.1:p.Ser290=
NM_001127511.2:c.816_823delinsTGTTTTGA	NP_001120983.2:p.Ser272=
NM_001354895.1:c.870_877delinsTGTTTTGA	NP_001341824.1:p.Ser290=
NM_001354896.1:c.870_877delinsTGTTTTGA	NP_001341825.1:p.Ser290=
NM_001354897.1:c.900_907delinsTGTTTTGA	NP_001341826.1:p.Ser300=
NM_001354898.1:c.795_802delinsTGTTTTGA	NP_001341827.1:p.Ser265=
NM_001354899.1:c.786_793delinsTGTTTTGA	NP_001341828.1:p.Ser262=
NM_001354900.1:c.693_700delinsTGTTTTGA	NP_001341829.1:p.Ser231=
NM_001354901.1:c.693_700delinsTGTTTTGA	NP_001341830.1:p.Ser231=
NM_001354902.1:c.900_907delinsTGTTTTGA	NP_001341831.1:p.Ser300=
NM_001354903.1:c.870_877delinsTGTTTTGA	NP_001341832.1:p.Ser290=
NM_001354904.1:c.795_802delinsTGTTTTGA	NP_001341833.1:p.Ser265=
NM_001354905.1:c.693_700delinsTGTTTTGA	NP_001341834.1:p.Ser231=
NM_001354906.1:c.21_28delinsTGTTTTGA	NP_001341835.1:p.Ser7=
NM_000038.6:c.870_877delinsTGTTTTGA MANE Select	NP_000029.2:p.Ser290=
NM_001127510.3:c.870_877delinsTGTTTTGA	NP_001120982.1:p.Ser290=
NM_001127511.3:c.816_823delinsTGTTTTGA	NP_001120983.2:p.Ser272=
NM_001354895.2:c.870_877delinsTGTTTTGA	NP_001341824.1:p.Ser290=
NM_001354896.2:c.870_877delinsTGTTTTGA	NP_001341825.1:p.Ser290=
NM_001354897.2:c.900_907delinsTGTTTTGA	NP_001341826.1:p.Ser300=
NM_001354898.2:c.795_802delinsTGTTTTGA	NP_001341827.1:p.Ser265=
NM_001354899.2:c.786_793delinsTGTTTTGA	NP_001341828.1:p.Ser262=
NM_001354900.2:c.693_700delinsTGTTTTGA	NP_001341829.1:p.Ser231=
NM_001354901.2:c.693_700delinsTGTTTTGA	NP_001341830.1:p.Ser231=
NM_001354902.2:c.900_907delinsTGTTTTGA	NP_001341831.1:p.Ser300=
NM_001354903.2:c.870_877delinsTGTTTTGA	NP_001341832.1:p.Ser290=
NM_001354904.2:c.795_802delinsTGTTTTGA	NP_001341833.1:p.Ser265=
NM_001354905.2:c.693_700delinsTGTTTTGA	NP_001341834.1:p.Ser231=
NM_001354906.2:c.21_28delinsTGTTTTGA	NP_001341835.1:p.Ser7=