Canonical Allele Identifier: CA1573478222

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112841350_112841351delinsAT , CM000667.2:g.112841350_112841351delinsAT	GRCh38
NC_000005.9:g.112177047_112177048delinsAT , CM000667.1:g.112177047_112177048delinsAT	GRCh37
NC_000005.8:g.112204946_112204947delinsAT	NCBI36
NG_008481.4:g.153830_153831delinsAT , LRG_130:g.153830_153831delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5810_5811delinsAT	ENSP00000473355.2:p.Asn1937=
ENST00000505350.2:c.*5762_*5763delinsAT	ENSP00000481752.1:n.*5762_*5763delinsAT
ENST00000507379.6:c.5702_5703delinsAT	ENSP00000423224.2:p.Asn1901=
ENST00000509732.6:c.5756_5757delinsAT	ENSP00000426541.2:p.Asn1919=
ENST00000512211.7:c.5756_5757delinsAT	ENSP00000423828.3:p.Asn1919=
ENST00000257430.9:c.5756_5757delinsAT MANE Select	ENSP00000257430.4:p.Asn1919=
ENST00000257430.8:c.5756_5757delinsAT	ENSP00000257430.4:p.Asn1919=
ENST00000508376.6:c.5756_5757delinsAT	ENSP00000427089.2:p.Asn1919=
ENST00000508624.5:c.*5078_*5079delinsAT	ENSP00000424265.1:n.*5078_*5079delinsAT
ENST00000520401.1:c.230+12378_230+12379delinsAT
NM_000038.5:c.5756_5757delinsAT	NP_000029.2:p.Asn1919=
NM_001127510.2:c.5756_5757delinsAT	NP_001120982.1:p.Asn1919=
NM_001127511.2:c.5702_5703delinsAT	NP_001120983.2:p.Asn1901=
NM_001354895.1:c.5756_5757delinsAT	NP_001341824.1:p.Asn1919=
NM_001354896.1:c.5810_5811delinsAT	NP_001341825.1:p.Asn1937=
NM_001354897.1:c.5786_5787delinsAT	NP_001341826.1:p.Asn1929=
NM_001354898.1:c.5681_5682delinsAT	NP_001341827.1:p.Asn1894=
NM_001354899.1:c.5672_5673delinsAT	NP_001341828.1:p.Asn1891=
NM_001354900.1:c.5633_5634delinsAT	NP_001341829.1:p.Asn1878=
NM_001354901.1:c.5579_5580delinsAT	NP_001341830.1:p.Asn1860=
NM_001354902.1:c.5483_5484delinsAT	NP_001341831.1:p.Asn1828=
NM_001354903.1:c.5453_5454delinsAT	NP_001341832.1:p.Asn1818=
NM_001354904.1:c.5378_5379delinsAT	NP_001341833.1:p.Asn1793=
NM_001354905.1:c.5276_5277delinsAT	NP_001341834.1:p.Asn1759=
NM_001354906.1:c.4907_4908delinsAT	NP_001341835.1:p.Asn1636=
NM_000038.6:c.5756_5757delinsAT MANE Select	NP_000029.2:p.Asn1919=
NM_001127510.3:c.5756_5757delinsAT	NP_001120982.1:p.Asn1919=
NM_001127511.3:c.5702_5703delinsAT	NP_001120983.2:p.Asn1901=
NM_001354895.2:c.5756_5757delinsAT	NP_001341824.1:p.Asn1919=
NM_001354896.2:c.5810_5811delinsAT	NP_001341825.1:p.Asn1937=
NM_001354897.2:c.5786_5787delinsAT	NP_001341826.1:p.Asn1929=
NM_001354898.2:c.5681_5682delinsAT	NP_001341827.1:p.Asn1894=
NM_001354899.2:c.5672_5673delinsAT	NP_001341828.1:p.Asn1891=
NM_001354900.2:c.5633_5634delinsAT	NP_001341829.1:p.Asn1878=
NM_001354901.2:c.5579_5580delinsAT	NP_001341830.1:p.Asn1860=
NM_001354902.2:c.5483_5484delinsAT	NP_001341831.1:p.Asn1828=
NM_001354903.2:c.5453_5454delinsAT	NP_001341832.1:p.Asn1818=
NM_001354904.2:c.5378_5379delinsAT	NP_001341833.1:p.Asn1793=
NM_001354905.2:c.5276_5277delinsAT	NP_001341834.1:p.Asn1759=
NM_001354906.2:c.4907_4908delinsAT	NP_001341835.1:p.Asn1636=