Canonical Allele Identifier: CA1573471092

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835073_112835074delinsCC , CM000667.2:g.112835073_112835074delinsCC	GRCh38
NC_000005.9:g.112170770_112170771delinsCC , CM000667.1:g.112170770_112170771delinsCC	GRCh37
NC_000005.8:g.112198669_112198670delinsCC	NCBI36
NG_008481.4:g.147553_147554delinsCC , LRG_130:g.147553_147554delinsCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1531_1532delinsCC	ENSP00000484935.2:n.1531_1532delinsCC
ENST00000504915.3:c.1920_1921delinsCC	ENSP00000473355.2:p.Tyr640=
ENST00000505350.2:c.*1872_*1873delinsCC	ENSP00000481752.1:n.*1872_*1873delinsCC
ENST00000507379.6:c.1812_1813delinsCC	ENSP00000423224.2:p.Tyr604=
ENST00000509732.6:c.1866_1867delinsCC	ENSP00000426541.2:p.Tyr622=
ENST00000512211.7:c.1866_1867delinsCC	ENSP00000423828.3:p.Tyr622=
ENST00000257430.9:c.1866_1867delinsCC MANE Select	ENSP00000257430.4:p.Tyr622=
ENST00000257430.8:c.1866_1867delinsCC	ENSP00000257430.4:p.Tyr622=
ENST00000502371.2:c.219_220delinsCC
ENST00000504915.2:c.555_556delinsCC	ENSP00000473355.1:p.Tyr185=
ENST00000507379.5:c.1812_1813delinsCC	ENSP00000423224.1:p.Tyr604=
ENST00000508376.6:c.1866_1867delinsCC	ENSP00000427089.2:p.Tyr622=
ENST00000508624.5:c.*1188_*1189delinsCC	ENSP00000424265.1:n.*1188_*1189delinsCC
ENST00000512211.6:c.1866_1867delinsCC	ENSP00000423828.2:p.Tyr622=
ENST00000520401.1:c.230+6101_230+6102delinsCC
NM_000038.5:c.1866_1867delinsCC	NP_000029.2:p.Tyr622=
NM_001127510.2:c.1866_1867delinsCC	NP_001120982.1:p.Tyr622=
NM_001127511.2:c.1812_1813delinsCC	NP_001120983.2:p.Tyr604=
NM_001354895.1:c.1866_1867delinsCC	NP_001341824.1:p.Tyr622=
NM_001354896.1:c.1920_1921delinsCC	NP_001341825.1:p.Tyr640=
NM_001354897.1:c.1896_1897delinsCC	NP_001341826.1:p.Tyr632=
NM_001354898.1:c.1791_1792delinsCC	NP_001341827.1:p.Tyr597=
NM_001354899.1:c.1782_1783delinsCC	NP_001341828.1:p.Tyr594=
NM_001354900.1:c.1743_1744delinsCC	NP_001341829.1:p.Tyr581=
NM_001354901.1:c.1689_1690delinsCC	NP_001341830.1:p.Tyr563=
NM_001354902.1:c.1593_1594delinsCC	NP_001341831.1:p.Tyr531=
NM_001354903.1:c.1563_1564delinsCC	NP_001341832.1:p.Tyr521=
NM_001354904.1:c.1488_1489delinsCC	NP_001341833.1:p.Tyr496=
NM_001354905.1:c.1386_1387delinsCC	NP_001341834.1:p.Tyr462=
NM_001354906.1:c.1017_1018delinsCC	NP_001341835.1:p.Tyr339=
NM_000038.6:c.1866_1867delinsCC MANE Select	NP_000029.2:p.Tyr622=
NM_001127510.3:c.1866_1867delinsCC	NP_001120982.1:p.Tyr622=
NM_001127511.3:c.1812_1813delinsCC	NP_001120983.2:p.Tyr604=
NM_001354895.2:c.1866_1867delinsCC	NP_001341824.1:p.Tyr622=
NM_001354896.2:c.1920_1921delinsCC	NP_001341825.1:p.Tyr640=
NM_001354897.2:c.1896_1897delinsCC	NP_001341826.1:p.Tyr632=
NM_001354898.2:c.1791_1792delinsCC	NP_001341827.1:p.Tyr597=
NM_001354899.2:c.1782_1783delinsCC	NP_001341828.1:p.Tyr594=
NM_001354900.2:c.1743_1744delinsCC	NP_001341829.1:p.Tyr581=
NM_001354901.2:c.1689_1690delinsCC	NP_001341830.1:p.Tyr563=
NM_001354902.2:c.1593_1594delinsCC	NP_001341831.1:p.Tyr531=
NM_001354903.2:c.1563_1564delinsCC	NP_001341832.1:p.Tyr521=
NM_001354904.2:c.1488_1489delinsCC	NP_001341833.1:p.Tyr496=
NM_001354905.2:c.1386_1387delinsCC	NP_001341834.1:p.Tyr462=
NM_001354906.2:c.1017_1018delinsCC	NP_001341835.1:p.Tyr339=