Canonical Allele Identifier: CA802044480

Gene: APC

Linked Data

• dbSNP Id: rs1239759650
• MyVariant Identifiers: chr5:g.112170105_112170106insTT (hg19) ; chr5:g.112834408_112834409insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112834416_112834417dup , CM000667.2:g.112834416_112834417dup	GRCh38
NC_000005.9:g.112170113_112170114dup , CM000667.1:g.112170113_112170114dup	GRCh37
NC_000005.8:g.112198012_112198013dup	NCBI36
NG_008481.4:g.146896_146897dup , LRG_130:g.146896_146897dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1409-535_1409-534dup	ENSP00000484935.2:n.1409-535_1409-534dup
ENST00000504915.3:c.1798-535_1798-534dup	ENSP00000473355.2:n.1798-535_1798-534dup
ENST00000505350.2:c.*1750-535_*1750-534dup	ENSP00000481752.1:n.*1750-535_*1750-534du...
ENST00000507379.6:c.1690-535_1690-534dup	ENSP00000423224.2:n.1690-535_1690-534dup
ENST00000509732.6:c.1744-535_1744-534dup	ENSP00000426541.2:n.1744-535_1744-534dup
ENST00000512211.7:c.1744-535_1744-534dup	ENSP00000423828.3:n.1744-535_1744-534dup
ENST00000257430.9:c.1744-535_1744-534dup MANE Select	ENSP00000257430.4:n.1744-535_1744-534dup
ENST00000257430.8:c.1744-535_1744-534dup	ENSP00000257430.4:n.1744-535_1744-534dup
ENST00000502371.2:c.97-535_97-534dup
ENST00000504915.2:c.433-535_433-534dup	ENSP00000473355.1:n.433-535_433-534dup
ENST00000507379.5:c.1690-535_1690-534dup	ENSP00000423224.1:n.1690-535_1690-534dup
ENST00000508376.6:c.1744-535_1744-534dup	ENSP00000427089.2:n.1744-535_1744-534dup
ENST00000508624.5:c.*1066-535_*1066-534dup	ENSP00000424265.1:n.*1066-535_*1066-534du...
ENST00000512211.6:c.1744-535_1744-534dup	ENSP00000423828.2:n.1744-535_1744-534dup
ENST00000520401.1:c.230+5444_230+5445dup
NM_000038.5:c.1744-535_1744-534dup	NP_000029.2:n.1744-535_1744-534dup
NM_001127510.2:c.1744-535_1744-534dup	NP_001120982.1:n.1744-535_1744-534dup
NM_001127511.2:c.1690-535_1690-534dup	NP_001120983.2:n.1690-535_1690-534dup
NM_001354895.1:c.1744-535_1744-534dup	NP_001341824.1:n.1744-535_1744-534dup
NM_001354896.1:c.1798-535_1798-534dup	NP_001341825.1:n.1798-535_1798-534dup
NM_001354897.1:c.1774-535_1774-534dup	NP_001341826.1:n.1774-535_1774-534dup
NM_001354898.1:c.1669-535_1669-534dup	NP_001341827.1:n.1669-535_1669-534dup
NM_001354899.1:c.1660-535_1660-534dup	NP_001341828.1:n.1660-535_1660-534dup
NM_001354900.1:c.1621-535_1621-534dup	NP_001341829.1:n.1621-535_1621-534dup
NM_001354901.1:c.1567-535_1567-534dup	NP_001341830.1:n.1567-535_1567-534dup
NM_001354902.1:c.1471-535_1471-534dup	NP_001341831.1:n.1471-535_1471-534dup
NM_001354903.1:c.1441-535_1441-534dup	NP_001341832.1:n.1441-535_1441-534dup
NM_001354904.1:c.1366-535_1366-534dup	NP_001341833.1:n.1366-535_1366-534dup
NM_001354905.1:c.1264-535_1264-534dup	NP_001341834.1:n.1264-535_1264-534dup
NM_001354906.1:c.895-535_895-534dup	NP_001341835.1:n.895-535_895-534dup
NM_000038.6:c.1744-535_1744-534dup MANE Select	NP_000029.2:n.1744-535_1744-534dup
NM_001127510.3:c.1744-535_1744-534dup	NP_001120982.1:n.1744-535_1744-534dup
NM_001127511.3:c.1690-535_1690-534dup	NP_001120983.2:n.1690-535_1690-534dup
NM_001354895.2:c.1744-535_1744-534dup	NP_001341824.1:n.1744-535_1744-534dup
NM_001354896.2:c.1798-535_1798-534dup	NP_001341825.1:n.1798-535_1798-534dup
NM_001354897.2:c.1774-535_1774-534dup	NP_001341826.1:n.1774-535_1774-534dup
NM_001354898.2:c.1669-535_1669-534dup	NP_001341827.1:n.1669-535_1669-534dup
NM_001354899.2:c.1660-535_1660-534dup	NP_001341828.1:n.1660-535_1660-534dup
NM_001354900.2:c.1621-535_1621-534dup	NP_001341829.1:n.1621-535_1621-534dup
NM_001354901.2:c.1567-535_1567-534dup	NP_001341830.1:n.1567-535_1567-534dup
NM_001354902.2:c.1471-535_1471-534dup	NP_001341831.1:n.1471-535_1471-534dup
NM_001354903.2:c.1441-535_1441-534dup	NP_001341832.1:n.1441-535_1441-534dup
NM_001354904.2:c.1366-535_1366-534dup	NP_001341833.1:n.1366-535_1366-534dup
NM_001354905.2:c.1264-535_1264-534dup	NP_001341834.1:n.1264-535_1264-534dup
NM_001354906.2:c.895-535_895-534dup	NP_001341835.1:n.895-535_895-534dup