Canonical Allele Identifier: CA1573442843
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707924_112707934delinsCTTCCTCGGCT , CM000667.2:g.112707924_112707934delinsCTTCCTCGGCT GRCh38
NC_000005.9:g.112043621_112043631delinsCTTCCTCGGCT , CM000667.1:g.112043621_112043631delinsCTTCCTCGGCT GRCh37
NC_000005.8:g.112071520_112071530delinsCTTCCTCGGCT NCBI36
NG_008481.4:g.20404_20414delinsCTTCCTCGGCT , LRG_130:g.20404_20414delinsCTTCCTCGGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000505350.2:c.165+42_165+52delinsCTTCCTCGGCT ENSP00000481752.1:n.165+42_165+52delinsCTTCCTCGGCT
ENST00000507379.6:c.165+42_165+52delinsCTTCCTCGGCT ENSP00000423224.2:n.165+42_165+52delinsCTTCCTCGGCT
ENST00000509732.6:c.-19+275_-19+285delinsCTTCCTCGGCT ENSP00000426541.2:n.-19+275_-19+285delinsCTTCCTCGGCT
ENST00000505350.1:c.165+42_165+52delinsCTTCCTCGGCT ENSP00000481752.1:n.165+42_165+52delinsCTTCCTCGGCT
ENST00000507379.5:c.165+42_165+52delinsCTTCCTCGGCT ENSP00000423224.1:n.165+42_165+52delinsCTTCCTCGGCT
ENST00000509732.5:c.-19+275_-19+285delinsCTTCCTCGGCT ENSP00000426541.1:n.-19+275_-19+285delinsCTTCCTCGGCT
NM_001127511.2:c.165+42_165+52delinsCTTCCTCGGCT NP_001120983.2:n.165+42_165+52delinsCTTCCTCGGCT
NM_001354895.1:c.-19+42_-19+52delinsCTTCCTCGGCT NP_001341824.1:n.-19+42_-19+52delinsCTTCCTCGGCT
NM_001354897.1:c.165+42_165+52delinsCTTCCTCGGCT NP_001341826.1:n.165+42_165+52delinsCTTCCTCGGCT
NM_001354902.1:c.165+42_165+52delinsCTTCCTCGGCT NP_001341831.1:n.165+42_165+52delinsCTTCCTCGGCT
NM_001127511.3:c.165+42_165+52delinsCTTCCTCGGCT NP_001120983.2:n.165+42_165+52delinsCTTCCTCGGCT
NM_001354895.2:c.-19+42_-19+52delinsCTTCCTCGGCT NP_001341824.1:n.-19+42_-19+52delinsCTTCCTCGGCT
NM_001354897.2:c.165+42_165+52delinsCTTCCTCGGCT NP_001341826.1:n.165+42_165+52delinsCTTCCTCGGCT
NM_001354902.2:c.165+42_165+52delinsCTTCCTCGGCT NP_001341831.1:n.165+42_165+52delinsCTTCCTCGGCT