Canonical Allele Identifier: CA562217596

Gene: APC

Linked Data

• dbSNP Id: rs1561569736
• gnomAD v2: 5-112170876-TTTATA-T
• gnomAD v4: 5-112835179-TTTATA-T
• MyVariant Identifiers: chr5:g.112170877_112170881del (hg19) ; chr5:g.112835180_112835184del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835183_112835187del , CM000667.2:g.112835183_112835187del	GRCh38
NC_000005.9:g.112170880_112170884del , CM000667.1:g.112170880_112170884del	GRCh37
NC_000005.8:g.112198779_112198783del	NCBI36
NG_008481.4:g.147663_147667del , LRG_130:g.147663_147667del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1623+18_1623+22del	ENSP00000484935.2:n.1623+18_1623+22del
ENST00000504915.3:c.2012+18_2012+22del	ENSP00000473355.2:n.2012+18_2012+22del
ENST00000505350.2:c.*1964+18_*1964+22del	ENSP00000481752.1:n.*1964+18_*1964+22del
ENST00000507379.6:c.1904+18_1904+22del	ENSP00000423224.2:n.1904+18_1904+22del
ENST00000509732.6:c.1958+18_1958+22del	ENSP00000426541.2:n.1958+18_1958+22del
ENST00000512211.7:c.1958+18_1958+22del	ENSP00000423828.3:n.1958+18_1958+22del
ENST00000257430.9:c.1958+18_1958+22del MANE Select	ENSP00000257430.4:n.1958+18_1958+22del
ENST00000257430.8:c.1958+18_1958+22del	ENSP00000257430.4:n.1958+18_1958+22del
ENST00000502371.2:c.311+18_311+22del
ENST00000504915.2:c.647+18_647+22del	ENSP00000473355.1:n.647+18_647+22del
ENST00000507379.5:c.1904+18_1904+22del	ENSP00000423224.1:n.1904+18_1904+22del
ENST00000508376.6:c.1958+18_1958+22del	ENSP00000427089.2:n.1958+18_1958+22del
ENST00000508624.5:c.*1280+18_*1280+22del	ENSP00000424265.1:n.*1280+18_*1280+22del
ENST00000512211.6:c.1958+18_1958+22del	ENSP00000423828.2:n.1958+18_1958+22del
ENST00000520401.1:c.230+6211_230+6215del
NM_000038.5:c.1958+18_1958+22del	NP_000029.2:n.1958+18_1958+22del
NM_001127510.2:c.1958+18_1958+22del	NP_001120982.1:n.1958+18_1958+22del
NM_001127511.2:c.1904+18_1904+22del	NP_001120983.2:n.1904+18_1904+22del
NM_001354895.1:c.1958+18_1958+22del	NP_001341824.1:n.1958+18_1958+22del
NM_001354896.1:c.2012+18_2012+22del	NP_001341825.1:n.2012+18_2012+22del
NM_001354897.1:c.1988+18_1988+22del	NP_001341826.1:n.1988+18_1988+22del
NM_001354898.1:c.1883+18_1883+22del	NP_001341827.1:n.1883+18_1883+22del
NM_001354899.1:c.1874+18_1874+22del	NP_001341828.1:n.1874+18_1874+22del
NM_001354900.1:c.1835+18_1835+22del	NP_001341829.1:n.1835+18_1835+22del
NM_001354901.1:c.1781+18_1781+22del	NP_001341830.1:n.1781+18_1781+22del
NM_001354902.1:c.1685+18_1685+22del	NP_001341831.1:n.1685+18_1685+22del
NM_001354903.1:c.1655+18_1655+22del	NP_001341832.1:n.1655+18_1655+22del
NM_001354904.1:c.1580+18_1580+22del	NP_001341833.1:n.1580+18_1580+22del
NM_001354905.1:c.1478+18_1478+22del	NP_001341834.1:n.1478+18_1478+22del
NM_001354906.1:c.1109+18_1109+22del	NP_001341835.1:n.1109+18_1109+22del
NM_000038.6:c.1958+18_1958+22del MANE Select	NP_000029.2:n.1958+18_1958+22del
NM_001127510.3:c.1958+18_1958+22del	NP_001120982.1:n.1958+18_1958+22del
NM_001127511.3:c.1904+18_1904+22del	NP_001120983.2:n.1904+18_1904+22del
NM_001354895.2:c.1958+18_1958+22del	NP_001341824.1:n.1958+18_1958+22del
NM_001354896.2:c.2012+18_2012+22del	NP_001341825.1:n.2012+18_2012+22del
NM_001354897.2:c.1988+18_1988+22del	NP_001341826.1:n.1988+18_1988+22del
NM_001354898.2:c.1883+18_1883+22del	NP_001341827.1:n.1883+18_1883+22del
NM_001354899.2:c.1874+18_1874+22del	NP_001341828.1:n.1874+18_1874+22del
NM_001354900.2:c.1835+18_1835+22del	NP_001341829.1:n.1835+18_1835+22del
NM_001354901.2:c.1781+18_1781+22del	NP_001341830.1:n.1781+18_1781+22del
NM_001354902.2:c.1685+18_1685+22del	NP_001341831.1:n.1685+18_1685+22del
NM_001354903.2:c.1655+18_1655+22del	NP_001341832.1:n.1655+18_1655+22del
NM_001354904.2:c.1580+18_1580+22del	NP_001341833.1:n.1580+18_1580+22del
NM_001354905.2:c.1478+18_1478+22del	NP_001341834.1:n.1478+18_1478+22del
NM_001354906.2:c.1109+18_1109+22del	NP_001341835.1:n.1109+18_1109+22del