Canonical Allele Identifier: CA2767942025

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840702_112840707del , CM000667.2:g.112840702_112840707del	GRCh38
NC_000005.9:g.112176399_112176404del , CM000667.1:g.112176399_112176404del	GRCh37
NC_000005.8:g.112204298_112204303del	NCBI36
NG_008481.4:g.153182_153187del , LRG_130:g.153182_153187del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5162_5167del	ENSP00000473355.2:p.Gly1721_Thr1723delinsAla
ENST00000505350.2:c.*5114_*5119del	ENSP00000481752.1:n.*5114_*5119del
ENST00000507379.6:c.5054_5059del	ENSP00000423224.2:p.Gly1685_Thr1687delinsAla
ENST00000509732.6:c.5108_5113del	ENSP00000426541.2:p.Gly1703_Thr1705delinsAla
ENST00000512211.7:c.5108_5113del	ENSP00000423828.3:p.Gly1703_Thr1705delinsAla
ENST00000257430.9:c.5108_5113del MANE Select	ENSP00000257430.4:p.Gly1703_Thr1705delinsAla
ENST00000257430.8:c.5108_5113del	ENSP00000257430.4:p.Gly1703_Thr1705delinsAla
ENST00000508376.6:c.5108_5113del	ENSP00000427089.2:p.Gly1703_Thr1705delinsAla
ENST00000508624.5:c.*4430_*4435del	ENSP00000424265.1:n.*4430_*4435del
ENST00000520401.1:c.230+11730_230+11735del
NM_000038.5:c.5108_5113del	NP_000029.2:p.Gly1703_Thr1705delinsAla
NM_001127510.2:c.5108_5113del	NP_001120982.1:p.Gly1703_Thr1705delinsAla
NM_001127511.2:c.5054_5059del	NP_001120983.2:p.Gly1685_Thr1687delinsAla
NM_001354895.1:c.5108_5113del	NP_001341824.1:p.Gly1703_Thr1705delinsAla
NM_001354896.1:c.5162_5167del	NP_001341825.1:p.Gly1721_Thr1723delinsAla
NM_001354897.1:c.5138_5143del	NP_001341826.1:p.Gly1713_Thr1715delinsAla
NM_001354898.1:c.5033_5038del	NP_001341827.1:p.Gly1678_Thr1680delinsAla
NM_001354899.1:c.5024_5029del	NP_001341828.1:p.Gly1675_Thr1677delinsAla
NM_001354900.1:c.4985_4990del	NP_001341829.1:p.Gly1662_Thr1664delinsAla
NM_001354901.1:c.4931_4936del	NP_001341830.1:p.Gly1644_Thr1646delinsAla
NM_001354902.1:c.4835_4840del	NP_001341831.1:p.Gly1612_Thr1614delinsAla
NM_001354903.1:c.4805_4810del	NP_001341832.1:p.Gly1602_Thr1604delinsAla
NM_001354904.1:c.4730_4735del	NP_001341833.1:p.Gly1577_Thr1579delinsAla
NM_001354905.1:c.4628_4633del	NP_001341834.1:p.Gly1543_Thr1545delinsAla
NM_001354906.1:c.4259_4264del	NP_001341835.1:p.Gly1420_Thr1422delinsAla
NM_000038.6:c.5108_5113del MANE Select	NP_000029.2:p.Gly1703_Thr1705delinsAla
NM_001127510.3:c.5108_5113del	NP_001120982.1:p.Gly1703_Thr1705delinsAla
NM_001127511.3:c.5054_5059del	NP_001120983.2:p.Gly1685_Thr1687delinsAla
NM_001354895.2:c.5108_5113del	NP_001341824.1:p.Gly1703_Thr1705delinsAla
NM_001354896.2:c.5162_5167del	NP_001341825.1:p.Gly1721_Thr1723delinsAla
NM_001354897.2:c.5138_5143del	NP_001341826.1:p.Gly1713_Thr1715delinsAla
NM_001354898.2:c.5033_5038del	NP_001341827.1:p.Gly1678_Thr1680delinsAla
NM_001354899.2:c.5024_5029del	NP_001341828.1:p.Gly1675_Thr1677delinsAla
NM_001354900.2:c.4985_4990del	NP_001341829.1:p.Gly1662_Thr1664delinsAla
NM_001354901.2:c.4931_4936del	NP_001341830.1:p.Gly1644_Thr1646delinsAla
NM_001354902.2:c.4835_4840del	NP_001341831.1:p.Gly1612_Thr1614delinsAla
NM_001354903.2:c.4805_4810del	NP_001341832.1:p.Gly1602_Thr1604delinsAla
NM_001354904.2:c.4730_4735del	NP_001341833.1:p.Gly1577_Thr1579delinsAla
NM_001354905.2:c.4628_4633del	NP_001341834.1:p.Gly1543_Thr1545delinsAla
NM_001354906.2:c.4259_4264del	NP_001341835.1:p.Gly1420_Thr1422delinsAla