Canonical Allele Identifier: CA1139770805

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112821894_112821897del , CM000667.2:g.112821894_112821897del	GRCh38
NC_000005.9:g.112157591_112157594del , CM000667.1:g.112157591_112157594del	GRCh37
NC_000005.8:g.112185490_112185493del	NCBI36
NG_008481.4:g.134374_134377del , LRG_130:g.134374_134377del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1313-2_1314del
ENST00000504915.3:c.1313-2_1314del
ENST00000505084.2:n.1369-2_1370del
ENST00000505350.2:c.*1319-2_*1320del
ENST00000507379.6:c.1259-2_1260del
ENST00000509732.6:c.1313-2_1314del
ENST00000512211.7:c.1313-2_1314del
ENST00000257430.9:c.1313-2_1314del
ENST00000257430.8:c.1313-2_1314del
ENST00000507379.5:c.1259-2_1260del
ENST00000508376.6:c.1313-2_1314del
ENST00000508624.5:c.*635-2_*636del
ENST00000512211.6:c.1313-2_1314del
NM_000038.5:c.1313-2_1314del
NM_001127510.2:c.1313-2_1314del
NM_001127511.2:c.1259-2_1260del
NM_001354895.1:c.1313-2_1314del
NM_001354896.1:c.1313-2_1314del
NM_001354897.1:c.1343-2_1344del
NM_001354898.1:c.1238-2_1239del
NM_001354899.1:c.1229-2_1230del
NM_001354900.1:c.1136-2_1137del
NM_001354901.1:c.1136-2_1137del
NM_001354902.1:c.1040-2_1041del
NM_001354903.1:c.1010-2_1011del
NM_001354904.1:c.935-2_936del
NM_001354905.1:c.833-2_834del
NM_001354906.1:c.464-2_465del
NM_000038.6:c.1313-2_1314del
NM_001127510.3:c.1313-2_1314del
NM_001127511.3:c.1259-2_1260del
NM_001354895.2:c.1313-2_1314del
NM_001354896.2:c.1313-2_1314del
NM_001354897.2:c.1343-2_1344del
NM_001354898.2:c.1238-2_1239del
NM_001354899.2:c.1229-2_1230del
NM_001354900.2:c.1136-2_1137del
NM_001354901.2:c.1136-2_1137del
NM_001354902.2:c.1040-2_1041del
NM_001354903.2:c.1010-2_1011del
NM_001354904.2:c.935-2_936del
NM_001354905.2:c.833-2_834del
NM_001354906.2:c.464-2_465del