Canonical Allele Identifier: CA2710010606

Gene: APC

Linked Data

• dbSNP Id: rs2149931144

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840661del , CM000667.2:g.112840661del	GRCh38
NC_000005.9:g.112176358del , CM000667.1:g.112176358del	GRCh37
NC_000005.8:g.112204257del	NCBI36
NG_008481.4:g.153141del , LRG_130:g.153141del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5121del	ENSP00000473355.2:p.Ile1708PhefsTer19
ENST00000505350.2:c.*5073del	ENSP00000481752.1:n.*5073del
ENST00000507379.6:c.5013del	ENSP00000423224.2:p.Ile1672PhefsTer19
ENST00000509732.6:c.5067del	ENSP00000426541.2:p.Ile1690PhefsTer19
ENST00000512211.7:c.5067del	ENSP00000423828.3:p.Ile1690PhefsTer19
ENST00000257430.9:c.5067del MANE Select	ENSP00000257430.4:p.Ile1690PhefsTer19
ENST00000257430.8:c.5067del	ENSP00000257430.4:p.Ile1690PhefsTer19
ENST00000508376.6:c.5067del	ENSP00000427089.2:p.Ile1690PhefsTer19
ENST00000508624.5:c.*4389del	ENSP00000424265.1:n.*4389del
ENST00000520401.1:c.230+11689del
NM_000038.5:c.5067del	NP_000029.2:p.Ile1690PhefsTer19
NM_001127510.2:c.5067del	NP_001120982.1:p.Ile1690PhefsTer19
NM_001127511.2:c.5013del	NP_001120983.2:p.Ile1672PhefsTer19
NM_001354895.1:c.5067del	NP_001341824.1:p.Ile1690PhefsTer19
NM_001354896.1:c.5121del	NP_001341825.1:p.Ile1708PhefsTer19
NM_001354897.1:c.5097del	NP_001341826.1:p.Ile1700PhefsTer19
NM_001354898.1:c.4992del	NP_001341827.1:p.Ile1665PhefsTer19
NM_001354899.1:c.4983del	NP_001341828.1:p.Ile1662PhefsTer19
NM_001354900.1:c.4944del	NP_001341829.1:p.Ile1649PhefsTer19
NM_001354901.1:c.4890del	NP_001341830.1:p.Ile1631PhefsTer19
NM_001354902.1:c.4794del	NP_001341831.1:p.Ile1599PhefsTer19
NM_001354903.1:c.4764del	NP_001341832.1:p.Ile1589PhefsTer19
NM_001354904.1:c.4689del	NP_001341833.1:p.Ile1564PhefsTer19
NM_001354905.1:c.4587del	NP_001341834.1:p.Ile1530PhefsTer19
NM_001354906.1:c.4218del	NP_001341835.1:p.Ile1407PhefsTer19
NM_000038.6:c.5067del MANE Select	NP_000029.2:p.Ile1690PhefsTer19
NM_001127510.3:c.5067del	NP_001120982.1:p.Ile1690PhefsTer19
NM_001127511.3:c.5013del	NP_001120983.2:p.Ile1672PhefsTer19
NM_001354895.2:c.5067del	NP_001341824.1:p.Ile1690PhefsTer19
NM_001354896.2:c.5121del	NP_001341825.1:p.Ile1708PhefsTer19
NM_001354897.2:c.5097del	NP_001341826.1:p.Ile1700PhefsTer19
NM_001354898.2:c.4992del	NP_001341827.1:p.Ile1665PhefsTer19
NM_001354899.2:c.4983del	NP_001341828.1:p.Ile1662PhefsTer19
NM_001354900.2:c.4944del	NP_001341829.1:p.Ile1649PhefsTer19
NM_001354901.2:c.4890del	NP_001341830.1:p.Ile1631PhefsTer19
NM_001354902.2:c.4794del	NP_001341831.1:p.Ile1599PhefsTer19
NM_001354903.2:c.4764del	NP_001341832.1:p.Ile1589PhefsTer19
NM_001354904.2:c.4689del	NP_001341833.1:p.Ile1564PhefsTer19
NM_001354905.2:c.4587del	NP_001341834.1:p.Ile1530PhefsTer19
NM_001354906.2:c.4218del	NP_001341835.1:p.Ile1407PhefsTer19