Canonical Allele Identifier: CA1080226271

Gene: APC

Linked Data

• dbSNP Id: rs1239759650
• gnomAD v3: 5-112834408-AT-A
• gnomAD v4: 5-112834408-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112834417del , CM000667.2:g.112834417del	GRCh38
NC_000005.9:g.112170114del , CM000667.1:g.112170114del	GRCh37
NC_000005.8:g.112198013del	NCBI36
NG_008481.4:g.146897del , LRG_130:g.146897del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1409-534del	ENSP00000484935.2:n.1409-534del
ENST00000504915.3:c.1798-534del	ENSP00000473355.2:n.1798-534del
ENST00000505350.2:c.*1750-534del	ENSP00000481752.1:n.*1750-534del
ENST00000507379.6:c.1690-534del	ENSP00000423224.2:n.1690-534del
ENST00000509732.6:c.1744-534del	ENSP00000426541.2:n.1744-534del
ENST00000512211.7:c.1744-534del	ENSP00000423828.3:n.1744-534del
ENST00000257430.9:c.1744-534del MANE Select	ENSP00000257430.4:n.1744-534del
ENST00000257430.8:c.1744-534del	ENSP00000257430.4:n.1744-534del
ENST00000502371.2:c.97-534del
ENST00000504915.2:c.433-534del	ENSP00000473355.1:n.433-534del
ENST00000507379.5:c.1690-534del	ENSP00000423224.1:n.1690-534del
ENST00000508376.6:c.1744-534del	ENSP00000427089.2:n.1744-534del
ENST00000508624.5:c.*1066-534del	ENSP00000424265.1:n.*1066-534del
ENST00000512211.6:c.1744-534del	ENSP00000423828.2:n.1744-534del
ENST00000520401.1:c.230+5445del
NM_000038.5:c.1744-534del	NP_000029.2:n.1744-534del
NM_001127510.2:c.1744-534del	NP_001120982.1:n.1744-534del
NM_001127511.2:c.1690-534del	NP_001120983.2:n.1690-534del
NM_001354895.1:c.1744-534del	NP_001341824.1:n.1744-534del
NM_001354896.1:c.1798-534del	NP_001341825.1:n.1798-534del
NM_001354897.1:c.1774-534del	NP_001341826.1:n.1774-534del
NM_001354898.1:c.1669-534del	NP_001341827.1:n.1669-534del
NM_001354899.1:c.1660-534del	NP_001341828.1:n.1660-534del
NM_001354900.1:c.1621-534del	NP_001341829.1:n.1621-534del
NM_001354901.1:c.1567-534del	NP_001341830.1:n.1567-534del
NM_001354902.1:c.1471-534del	NP_001341831.1:n.1471-534del
NM_001354903.1:c.1441-534del	NP_001341832.1:n.1441-534del
NM_001354904.1:c.1366-534del	NP_001341833.1:n.1366-534del
NM_001354905.1:c.1264-534del	NP_001341834.1:n.1264-534del
NM_001354906.1:c.895-534del	NP_001341835.1:n.895-534del
NM_000038.6:c.1744-534del MANE Select	NP_000029.2:n.1744-534del
NM_001127510.3:c.1744-534del	NP_001120982.1:n.1744-534del
NM_001127511.3:c.1690-534del	NP_001120983.2:n.1690-534del
NM_001354895.2:c.1744-534del	NP_001341824.1:n.1744-534del
NM_001354896.2:c.1798-534del	NP_001341825.1:n.1798-534del
NM_001354897.2:c.1774-534del	NP_001341826.1:n.1774-534del
NM_001354898.2:c.1669-534del	NP_001341827.1:n.1669-534del
NM_001354899.2:c.1660-534del	NP_001341828.1:n.1660-534del
NM_001354900.2:c.1621-534del	NP_001341829.1:n.1621-534del
NM_001354901.2:c.1567-534del	NP_001341830.1:n.1567-534del
NM_001354902.2:c.1471-534del	NP_001341831.1:n.1471-534del
NM_001354903.2:c.1441-534del	NP_001341832.1:n.1441-534del
NM_001354904.2:c.1366-534del	NP_001341833.1:n.1366-534del
NM_001354905.2:c.1264-534del	NP_001341834.1:n.1264-534del
NM_001354906.2:c.895-534del	NP_001341835.1:n.895-534del