Canonical Allele Identifier: CA16027001

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838183C>A , CM000667.2:g.112838183C>A	GRCh38
NC_000005.9:g.112173880C>A , CM000667.1:g.112173880C>A	GRCh37
NC_000005.8:g.112201779C>A	NCBI36
NG_008481.4:g.150663C>A , LRG_130:g.150663C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2254C>A	ENSP00000484935.2:n.2254C>A
ENST00000504915.3:c.2643C>A	ENSP00000473355.2:p.Tyr881Ter
ENST00000505350.2:c.*2595C>A	ENSP00000481752.1:n.*2595C>A
ENST00000507379.6:c.2535C>A	ENSP00000423224.2:p.Tyr845Ter
ENST00000509732.6:c.2589C>A	ENSP00000426541.2:p.Tyr863Ter
ENST00000512211.7:c.2589C>A	ENSP00000423828.3:p.Tyr863Ter
ENST00000257430.9:c.2589C>A MANE Select	ENSP00000257430.4:p.Tyr863Ter
ENST00000257430.8:c.2589C>A	ENSP00000257430.4:p.Tyr863Ter
ENST00000502371.2:c.942C>A
ENST00000507379.5:c.2535C>A	ENSP00000423224.1:p.Tyr845Ter
ENST00000508376.6:c.2589C>A	ENSP00000427089.2:p.Tyr863Ter
ENST00000508624.5:c.*1911C>A	ENSP00000424265.1:n.*1911C>A
ENST00000512211.6:c.2589C>A	ENSP00000423828.2:p.Tyr863Ter
ENST00000520401.1:c.230+9211C>A
NM_000038.5:c.2589C>A	NP_000029.2:p.Tyr863Ter
NM_001127510.2:c.2589C>A	NP_001120982.1:p.Tyr863Ter
NM_001127511.2:c.2535C>A	NP_001120983.2:p.Tyr845Ter
NM_001354895.1:c.2589C>A	NP_001341824.1:p.Tyr863Ter
NM_001354896.1:c.2643C>A	NP_001341825.1:p.Tyr881Ter
NM_001354897.1:c.2619C>A	NP_001341826.1:p.Tyr873Ter
NM_001354898.1:c.2514C>A	NP_001341827.1:p.Tyr838Ter
NM_001354899.1:c.2505C>A	NP_001341828.1:p.Tyr835Ter
NM_001354900.1:c.2466C>A	NP_001341829.1:p.Tyr822Ter
NM_001354901.1:c.2412C>A	NP_001341830.1:p.Tyr804Ter
NM_001354902.1:c.2316C>A	NP_001341831.1:p.Tyr772Ter
NM_001354903.1:c.2286C>A	NP_001341832.1:p.Tyr762Ter
NM_001354904.1:c.2211C>A	NP_001341833.1:p.Tyr737Ter
NM_001354905.1:c.2109C>A	NP_001341834.1:p.Tyr703Ter
NM_001354906.1:c.1740C>A	NP_001341835.1:p.Tyr580Ter
NM_000038.6:c.2589C>A MANE Select	NP_000029.2:p.Tyr863Ter
NM_001127510.3:c.2589C>A	NP_001120982.1:p.Tyr863Ter
NM_001127511.3:c.2535C>A	NP_001120983.2:p.Tyr845Ter
NM_001354895.2:c.2589C>A	NP_001341824.1:p.Tyr863Ter
NM_001354896.2:c.2643C>A	NP_001341825.1:p.Tyr881Ter
NM_001354897.2:c.2619C>A	NP_001341826.1:p.Tyr873Ter
NM_001354898.2:c.2514C>A	NP_001341827.1:p.Tyr838Ter
NM_001354899.2:c.2505C>A	NP_001341828.1:p.Tyr835Ter
NM_001354900.2:c.2466C>A	NP_001341829.1:p.Tyr822Ter
NM_001354901.2:c.2412C>A	NP_001341830.1:p.Tyr804Ter
NM_001354902.2:c.2316C>A	NP_001341831.1:p.Tyr772Ter
NM_001354903.2:c.2286C>A	NP_001341832.1:p.Tyr762Ter
NM_001354904.2:c.2211C>A	NP_001341833.1:p.Tyr737Ter
NM_001354905.2:c.2109C>A	NP_001341834.1:p.Tyr703Ter
NM_001354906.2:c.1740C>A	NP_001341835.1:p.Tyr580Ter