Canonical Allele Identifier: CA16038855

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843665A>G , CM000667.2:g.112843665A>G	GRCh38
NC_000005.9:g.112179362A>G , CM000667.1:g.112179362A>G	GRCh37
NC_000005.8:g.112207261A>G	NCBI36
NG_008481.4:g.156145A>G , LRG_130:g.156145A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.8071A>G MANE Select	NP_000029.2:p.Asn2691Asp
ENST00000257430.9:c.8071A>G MANE Select	ENSP00000257430.4:p.Asn2691Asp
NM_000038.5:c.8071A>G	NP_000029.2:p.Asn2691Asp
NM_001127510.2:c.8071A>G	NP_001120982.1:p.Asn2691Asp
NM_001127510.3:c.8071A>G	NP_001120982.1:p.Asn2691Asp
NM_001127511.2:c.8017A>G	NP_001120983.2:p.Asn2673Asp
NM_001127511.3:c.8017A>G	NP_001120983.2:p.Asn2673Asp
NM_001354895.1:c.8071A>G	NP_001341824.1:p.Asn2691Asp
NM_001354895.2:c.8071A>G	NP_001341824.1:p.Asn2691Asp
NM_001354896.1:c.8125A>G	NP_001341825.1:p.Asn2709Asp
NM_001354896.2:c.8125A>G	NP_001341825.1:p.Asn2709Asp
NM_001354897.1:c.8101A>G	NP_001341826.1:p.Asn2701Asp
NM_001354897.2:c.8101A>G	NP_001341826.1:p.Asn2701Asp
NM_001354898.1:c.7996A>G	NP_001341827.1:p.Asn2666Asp
NM_001354898.2:c.7996A>G	NP_001341827.1:p.Asn2666Asp
NM_001354899.1:c.7987A>G	NP_001341828.1:p.Asn2663Asp
NM_001354899.2:c.7987A>G	NP_001341828.1:p.Asn2663Asp
NM_001354900.1:c.7948A>G	NP_001341829.1:p.Asn2650Asp
NM_001354900.2:c.7948A>G	NP_001341829.1:p.Asn2650Asp
NM_001354901.1:c.7894A>G	NP_001341830.1:p.Asn2632Asp
NM_001354901.2:c.7894A>G	NP_001341830.1:p.Asn2632Asp
NM_001354902.1:c.7798A>G	NP_001341831.1:p.Asn2600Asp
NM_001354902.2:c.7798A>G	NP_001341831.1:p.Asn2600Asp
NM_001354903.1:c.7768A>G	NP_001341832.1:p.Asn2590Asp
NM_001354903.2:c.7768A>G	NP_001341832.1:p.Asn2590Asp
NM_001354904.1:c.7693A>G	NP_001341833.1:p.Asn2565Asp
NM_001354904.2:c.7693A>G	NP_001341833.1:p.Asn2565Asp
NM_001354905.1:c.7591A>G	NP_001341834.1:p.Asn2531Asp
NM_001354905.2:c.7591A>G	NP_001341834.1:p.Asn2531Asp
NM_001354906.1:c.7222A>G	NP_001341835.1:p.Asn2408Asp
NM_001354906.2:c.7222A>G	NP_001341835.1:p.Asn2408Asp
ENST00000257430.8:c.8071A>G	ENSP00000257430.4:p.Asn2691Asp
ENST00000504915.3:c.8125A>G	ENSP00000473355.2:p.Asn2709Asp
ENST00000505350.2:c.*8077A>G	ENSP00000481752.1:n.*8077A>G
ENST00000507379.6:c.8017A>G	ENSP00000423224.2:p.Asn2673Asp
ENST00000508376.6:c.8071A>G	ENSP00000427089.2:p.Asn2691Asp
ENST00000509732.6:c.8071A>G	ENSP00000426541.2:p.Asn2691Asp
ENST00000512211.7:c.8071A>G	ENSP00000423828.3:p.Asn2691Asp
ENST00000520401.1:c.231-12984A>G