Canonical Allele Identifier: CA350548

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838873T>G , CM000667.2:g.112838873T>G	GRCh38
NC_000005.9:g.112174570T>G , CM000667.1:g.112174570T>G	GRCh37
NC_000005.8:g.112202469T>G	NCBI36
NG_008481.4:g.151353T>G , LRG_130:g.151353T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2944T>G	ENSP00000484935.2:n.2944T>G
ENST00000504915.3:c.3333T>G	ENSP00000473355.2:p.Phe1111Leu
ENST00000505350.2:c.*3285T>G	ENSP00000481752.1:n.*3285T>G
ENST00000507379.6:c.3225T>G	ENSP00000423224.2:p.Phe1075Leu
ENST00000509732.6:c.3279T>G	ENSP00000426541.2:p.Phe1093Leu
ENST00000512211.7:c.3279T>G	ENSP00000423828.3:p.Phe1093Leu
ENST00000257430.9:c.3279T>G MANE Select	ENSP00000257430.4:p.Phe1093Leu
ENST00000257430.8:c.3279T>G	ENSP00000257430.4:p.Phe1093Leu
ENST00000502371.2:c.1632T>G
ENST00000507379.5:c.3225T>G	ENSP00000423224.1:p.Phe1075Leu
ENST00000508376.6:c.3279T>G	ENSP00000427089.2:p.Phe1093Leu
ENST00000508624.5:c.*2601T>G	ENSP00000424265.1:n.*2601T>G
ENST00000512211.6:c.3279T>G	ENSP00000423828.2:p.Phe1093Leu
ENST00000520401.1:c.230+9901T>G
NM_000038.5:c.3279T>G	NP_000029.2:p.Phe1093Leu
NM_001127510.2:c.3279T>G	NP_001120982.1:p.Phe1093Leu
NM_001127511.2:c.3225T>G	NP_001120983.2:p.Phe1075Leu
NM_001354895.1:c.3279T>G	NP_001341824.1:p.Phe1093Leu
NM_001354896.1:c.3333T>G	NP_001341825.1:p.Phe1111Leu
NM_001354897.1:c.3309T>G	NP_001341826.1:p.Phe1103Leu
NM_001354898.1:c.3204T>G	NP_001341827.1:p.Phe1068Leu
NM_001354899.1:c.3195T>G	NP_001341828.1:p.Phe1065Leu
NM_001354900.1:c.3156T>G	NP_001341829.1:p.Phe1052Leu
NM_001354901.1:c.3102T>G	NP_001341830.1:p.Phe1034Leu
NM_001354902.1:c.3006T>G	NP_001341831.1:p.Phe1002Leu
NM_001354903.1:c.2976T>G	NP_001341832.1:p.Phe992Leu
NM_001354904.1:c.2901T>G	NP_001341833.1:p.Phe967Leu
NM_001354905.1:c.2799T>G	NP_001341834.1:p.Phe933Leu
NM_001354906.1:c.2430T>G	NP_001341835.1:p.Phe810Leu
NM_000038.6:c.3279T>G MANE Select	NP_000029.2:p.Phe1093Leu
NM_001127510.3:c.3279T>G	NP_001120982.1:p.Phe1093Leu
NM_001127511.3:c.3225T>G	NP_001120983.2:p.Phe1075Leu
NM_001354895.2:c.3279T>G	NP_001341824.1:p.Phe1093Leu
NM_001354896.2:c.3333T>G	NP_001341825.1:p.Phe1111Leu
NM_001354897.2:c.3309T>G	NP_001341826.1:p.Phe1103Leu
NM_001354898.2:c.3204T>G	NP_001341827.1:p.Phe1068Leu
NM_001354899.2:c.3195T>G	NP_001341828.1:p.Phe1065Leu
NM_001354900.2:c.3156T>G	NP_001341829.1:p.Phe1052Leu
NM_001354901.2:c.3102T>G	NP_001341830.1:p.Phe1034Leu
NM_001354902.2:c.3006T>G	NP_001341831.1:p.Phe1002Leu
NM_001354903.2:c.2976T>G	NP_001341832.1:p.Phe992Leu
NM_001354904.2:c.2901T>G	NP_001341833.1:p.Phe967Leu
NM_001354905.2:c.2799T>G	NP_001341834.1:p.Phe933Leu
NM_001354906.2:c.2430T>G	NP_001341835.1:p.Phe810Leu