Canonical Allele Identifier: CA2709983804

Gene: APC

Linked Data

• dbSNP Id: rs2149844777

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835178T>A , CM000667.2:g.112835178T>A	GRCh38
NC_000005.9:g.112170875T>A , CM000667.1:g.112170875T>A	GRCh37
NC_000005.8:g.112198774T>A	NCBI36
NG_008481.4:g.147658T>A , LRG_130:g.147658T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1623+13T>A	ENSP00000484935.2:n.1623+13T>A
ENST00000504915.3:c.2012+13T>A	ENSP00000473355.2:n.2012+13T>A
ENST00000505350.2:c.*1964+13T>A	ENSP00000481752.1:n.*1964+13T>A
ENST00000507379.6:c.1904+13T>A	ENSP00000423224.2:n.1904+13T>A
ENST00000509732.6:c.1958+13T>A	ENSP00000426541.2:n.1958+13T>A
ENST00000512211.7:c.1958+13T>A	ENSP00000423828.3:n.1958+13T>A
ENST00000257430.9:c.1958+13T>A MANE Select	ENSP00000257430.4:n.1958+13T>A
ENST00000257430.8:c.1958+13T>A	ENSP00000257430.4:n.1958+13T>A
ENST00000502371.2:c.311+13T>A
ENST00000504915.2:c.647+13T>A	ENSP00000473355.1:n.647+13T>A
ENST00000507379.5:c.1904+13T>A	ENSP00000423224.1:n.1904+13T>A
ENST00000508376.6:c.1958+13T>A	ENSP00000427089.2:n.1958+13T>A
ENST00000508624.5:c.*1280+13T>A	ENSP00000424265.1:n.*1280+13T>A
ENST00000512211.6:c.1958+13T>A	ENSP00000423828.2:n.1958+13T>A
ENST00000520401.1:c.230+6206T>A
NM_000038.5:c.1958+13T>A	NP_000029.2:n.1958+13T>A
NM_001127510.2:c.1958+13T>A	NP_001120982.1:n.1958+13T>A
NM_001127511.2:c.1904+13T>A	NP_001120983.2:n.1904+13T>A
NM_001354895.1:c.1958+13T>A	NP_001341824.1:n.1958+13T>A
NM_001354896.1:c.2012+13T>A	NP_001341825.1:n.2012+13T>A
NM_001354897.1:c.1988+13T>A	NP_001341826.1:n.1988+13T>A
NM_001354898.1:c.1883+13T>A	NP_001341827.1:n.1883+13T>A
NM_001354899.1:c.1874+13T>A	NP_001341828.1:n.1874+13T>A
NM_001354900.1:c.1835+13T>A	NP_001341829.1:n.1835+13T>A
NM_001354901.1:c.1781+13T>A	NP_001341830.1:n.1781+13T>A
NM_001354902.1:c.1685+13T>A	NP_001341831.1:n.1685+13T>A
NM_001354903.1:c.1655+13T>A	NP_001341832.1:n.1655+13T>A
NM_001354904.1:c.1580+13T>A	NP_001341833.1:n.1580+13T>A
NM_001354905.1:c.1478+13T>A	NP_001341834.1:n.1478+13T>A
NM_001354906.1:c.1109+13T>A	NP_001341835.1:n.1109+13T>A
NM_000038.6:c.1958+13T>A MANE Select	NP_000029.2:n.1958+13T>A
NM_001127510.3:c.1958+13T>A	NP_001120982.1:n.1958+13T>A
NM_001127511.3:c.1904+13T>A	NP_001120983.2:n.1904+13T>A
NM_001354895.2:c.1958+13T>A	NP_001341824.1:n.1958+13T>A
NM_001354896.2:c.2012+13T>A	NP_001341825.1:n.2012+13T>A
NM_001354897.2:c.1988+13T>A	NP_001341826.1:n.1988+13T>A
NM_001354898.2:c.1883+13T>A	NP_001341827.1:n.1883+13T>A
NM_001354899.2:c.1874+13T>A	NP_001341828.1:n.1874+13T>A
NM_001354900.2:c.1835+13T>A	NP_001341829.1:n.1835+13T>A
NM_001354901.2:c.1781+13T>A	NP_001341830.1:n.1781+13T>A
NM_001354902.2:c.1685+13T>A	NP_001341831.1:n.1685+13T>A
NM_001354903.2:c.1655+13T>A	NP_001341832.1:n.1655+13T>A
NM_001354904.2:c.1580+13T>A	NP_001341833.1:n.1580+13T>A
NM_001354905.2:c.1478+13T>A	NP_001341834.1:n.1478+13T>A
NM_001354906.2:c.1109+13T>A	NP_001341835.1:n.1109+13T>A