Canonical Allele Identifier: CA007349

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112837891C>T , CM000667.2:g.112837891C>T	GRCh38
NC_000005.9:g.112173588C>T , CM000667.1:g.112173588C>T	GRCh37
NC_000005.8:g.112201487C>T	NCBI36
NG_008481.4:g.150371C>T , LRG_130:g.150371C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.2297C>T MANE Select	NP_000029.2:p.Ala766Val
ENST00000257430.9:c.2297C>T MANE Select	ENSP00000257430.4:p.Ala766Val
NM_000038.5:c.2297C>T	NP_000029.2:p.Ala766Val
NM_001127510.2:c.2297C>T	NP_001120982.1:p.Ala766Val
NM_001127510.3:c.2297C>T	NP_001120982.1:p.Ala766Val
NM_001127511.2:c.2243C>T	NP_001120983.2:p.Ala748Val
NM_001127511.3:c.2243C>T	NP_001120983.2:p.Ala748Val
NM_001354895.1:c.2297C>T	NP_001341824.1:p.Ala766Val
NM_001354895.2:c.2297C>T	NP_001341824.1:p.Ala766Val
NM_001354896.1:c.2351C>T	NP_001341825.1:p.Ala784Val
NM_001354896.2:c.2351C>T	NP_001341825.1:p.Ala784Val
NM_001354897.1:c.2327C>T	NP_001341826.1:p.Ala776Val
NM_001354897.2:c.2327C>T	NP_001341826.1:p.Ala776Val
NM_001354898.1:c.2222C>T	NP_001341827.1:p.Ala741Val
NM_001354898.2:c.2222C>T	NP_001341827.1:p.Ala741Val
NM_001354899.1:c.2213C>T	NP_001341828.1:p.Ala738Val
NM_001354899.2:c.2213C>T	NP_001341828.1:p.Ala738Val
NM_001354900.1:c.2174C>T	NP_001341829.1:p.Ala725Val
NM_001354900.2:c.2174C>T	NP_001341829.1:p.Ala725Val
NM_001354901.1:c.2120C>T	NP_001341830.1:p.Ala707Val
NM_001354901.2:c.2120C>T	NP_001341830.1:p.Ala707Val
NM_001354902.1:c.2024C>T	NP_001341831.1:p.Ala675Val
NM_001354902.2:c.2024C>T	NP_001341831.1:p.Ala675Val
NM_001354903.1:c.1994C>T	NP_001341832.1:p.Ala665Val
NM_001354903.2:c.1994C>T	NP_001341832.1:p.Ala665Val
NM_001354904.1:c.1919C>T	NP_001341833.1:p.Ala640Val
NM_001354904.2:c.1919C>T	NP_001341833.1:p.Ala640Val
NM_001354905.1:c.1817C>T	NP_001341834.1:p.Ala606Val
NM_001354905.2:c.1817C>T	NP_001341834.1:p.Ala606Val
NM_001354906.1:c.1448C>T	NP_001341835.1:p.Ala483Val
NM_001354906.2:c.1448C>T	NP_001341835.1:p.Ala483Val
ENST00000257430.8:c.2297C>T	ENSP00000257430.4:p.Ala766Val
ENST00000502371.2:c.650C>T
ENST00000502371.3:c.1962C>T	ENSP00000484935.2:n.1962C>T
ENST00000504915.3:c.2351C>T	ENSP00000473355.2:p.Ala784Val
ENST00000505350.2:c.*2303C>T	ENSP00000481752.1:n.*2303C>T
ENST00000507379.5:c.2243C>T	ENSP00000423224.1:p.Ala748Val
ENST00000507379.6:c.2243C>T	ENSP00000423224.2:p.Ala748Val
ENST00000508376.6:c.2297C>T	ENSP00000427089.2:p.Ala766Val
ENST00000508624.5:c.*1619C>T	ENSP00000424265.1:n.*1619C>T
ENST00000509732.6:c.2297C>T	ENSP00000426541.2:p.Ala766Val
ENST00000512211.6:c.2297C>T	ENSP00000423828.2:p.Ala766Val
ENST00000512211.7:c.2297C>T	ENSP00000423828.3:p.Ala766Val
ENST00000520401.1:c.230+8919C>T