Canonical Allele Identifier: CA445757381

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112164570_112164571insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828873_112828874insT , CM000667.2:g.112828873_112828874insT	GRCh38
NC_000005.9:g.112164570_112164571insT , CM000667.1:g.112164570_112164571insT	GRCh37
NC_000005.8:g.112192469_112192470insT	NCBI36
NG_008481.4:g.141353_141354insT , LRG_130:g.141353_141354insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1409-6078_1409-6077insT	ENSP00000484935.2:n.1409-6078_1409-6077in...
ENST00000504915.3:c.1698_1699insT	ENSP00000473355.2:p.Arg567Ter
ENST00000505084.2:n.1700_1701insT
ENST00000505350.2:c.*1650_*1651insT	ENSP00000481752.1:n.*1650_*1651insT
ENST00000507379.6:c.1590_1591insT	ENSP00000423224.2:p.Arg531Ter
ENST00000509732.6:c.1644_1645insT	ENSP00000426541.2:p.Arg549Ter
ENST00000512211.7:c.1644_1645insT	ENSP00000423828.3:p.Arg549Ter
ENST00000257430.9:c.1644_1645insT MANE Select	ENSP00000257430.4:p.Arg549Ter
ENST00000257430.8:c.1644_1645insT	ENSP00000257430.4:p.Arg549Ter
ENST00000502371.2:c.97-6078_97-6077insT
ENST00000504915.2:c.333_334insT	ENSP00000473355.1:p.Arg112Ter
ENST00000505084.1:n.131_132insT
ENST00000507379.5:c.1590_1591insT	ENSP00000423224.1:p.Arg531Ter
ENST00000508376.6:c.1644_1645insT	ENSP00000427089.2:p.Arg549Ter
ENST00000508624.5:c.*966_*967insT	ENSP00000424265.1:n.*966_*967insT
ENST00000512211.6:c.1644_1645insT	ENSP00000423828.2:p.Arg549Ter
ENST00000520401.1:c.131_132insT
NM_000038.5:c.1644_1645insT	NP_000029.2:p.Arg549Ter
NM_001127510.2:c.1644_1645insT	NP_001120982.1:p.Arg549Ter
NM_001127511.2:c.1590_1591insT	NP_001120983.2:p.Arg531Ter
NM_001354895.1:c.1644_1645insT	NP_001341824.1:p.Arg549Ter
NM_001354896.1:c.1698_1699insT	NP_001341825.1:p.Arg567Ter
NM_001354897.1:c.1674_1675insT	NP_001341826.1:p.Arg559Ter
NM_001354898.1:c.1569_1570insT	NP_001341827.1:p.Arg524Ter
NM_001354899.1:c.1560_1561insT	NP_001341828.1:p.Arg521Ter
NM_001354900.1:c.1521_1522insT	NP_001341829.1:p.Arg508Ter
NM_001354901.1:c.1467_1468insT	NP_001341830.1:p.Arg490Ter
NM_001354902.1:c.1371_1372insT	NP_001341831.1:p.Arg458Ter
NM_001354903.1:c.1341_1342insT	NP_001341832.1:p.Arg448Ter
NM_001354904.1:c.1266_1267insT	NP_001341833.1:p.Arg423Ter
NM_001354905.1:c.1164_1165insT	NP_001341834.1:p.Arg389Ter
NM_001354906.1:c.795_796insT	NP_001341835.1:p.Arg266Ter
NM_000038.6:c.1644_1645insT MANE Select	NP_000029.2:p.Arg549Ter
NM_001127510.3:c.1644_1645insT	NP_001120982.1:p.Arg549Ter
NM_001127511.3:c.1590_1591insT	NP_001120983.2:p.Arg531Ter
NM_001354895.2:c.1644_1645insT	NP_001341824.1:p.Arg549Ter
NM_001354896.2:c.1698_1699insT	NP_001341825.1:p.Arg567Ter
NM_001354897.2:c.1674_1675insT	NP_001341826.1:p.Arg559Ter
NM_001354898.2:c.1569_1570insT	NP_001341827.1:p.Arg524Ter
NM_001354899.2:c.1560_1561insT	NP_001341828.1:p.Arg521Ter
NM_001354900.2:c.1521_1522insT	NP_001341829.1:p.Arg508Ter
NM_001354901.2:c.1467_1468insT	NP_001341830.1:p.Arg490Ter
NM_001354902.2:c.1371_1372insT	NP_001341831.1:p.Arg458Ter
NM_001354903.2:c.1341_1342insT	NP_001341832.1:p.Arg448Ter
NM_001354904.2:c.1266_1267insT	NP_001341833.1:p.Arg423Ter
NM_001354905.2:c.1164_1165insT	NP_001341834.1:p.Arg389Ter
NM_001354906.2:c.795_796insT	NP_001341835.1:p.Arg266Ter