Canonical Allele Identifier: CA16033081

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840971G>A , CM000667.2:g.112840971G>A	GRCh38
NC_000005.9:g.112176668G>A , CM000667.1:g.112176668G>A	GRCh37
NC_000005.8:g.112204567G>A	NCBI36
NG_008481.4:g.153451G>A , LRG_130:g.153451G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.5377G>A MANE Select	NP_000029.2:p.Ala1793Thr
ENST00000257430.9:c.5377G>A MANE Select	ENSP00000257430.4:p.Ala1793Thr
NM_000038.5:c.5377G>A	NP_000029.2:p.Ala1793Thr
NM_001127510.2:c.5377G>A	NP_001120982.1:p.Ala1793Thr
NM_001127510.3:c.5377G>A	NP_001120982.1:p.Ala1793Thr
NM_001127511.2:c.5323G>A	NP_001120983.2:p.Ala1775Thr
NM_001127511.3:c.5323G>A	NP_001120983.2:p.Ala1775Thr
NM_001354895.1:c.5377G>A	NP_001341824.1:p.Ala1793Thr
NM_001354895.2:c.5377G>A	NP_001341824.1:p.Ala1793Thr
NM_001354896.1:c.5431G>A	NP_001341825.1:p.Ala1811Thr
NM_001354896.2:c.5431G>A	NP_001341825.1:p.Ala1811Thr
NM_001354897.1:c.5407G>A	NP_001341826.1:p.Ala1803Thr
NM_001354897.2:c.5407G>A	NP_001341826.1:p.Ala1803Thr
NM_001354898.1:c.5302G>A	NP_001341827.1:p.Ala1768Thr
NM_001354898.2:c.5302G>A	NP_001341827.1:p.Ala1768Thr
NM_001354899.1:c.5293G>A	NP_001341828.1:p.Ala1765Thr
NM_001354899.2:c.5293G>A	NP_001341828.1:p.Ala1765Thr
NM_001354900.1:c.5254G>A	NP_001341829.1:p.Ala1752Thr
NM_001354900.2:c.5254G>A	NP_001341829.1:p.Ala1752Thr
NM_001354901.1:c.5200G>A	NP_001341830.1:p.Ala1734Thr
NM_001354901.2:c.5200G>A	NP_001341830.1:p.Ala1734Thr
NM_001354902.1:c.5104G>A	NP_001341831.1:p.Ala1702Thr
NM_001354902.2:c.5104G>A	NP_001341831.1:p.Ala1702Thr
NM_001354903.1:c.5074G>A	NP_001341832.1:p.Ala1692Thr
NM_001354903.2:c.5074G>A	NP_001341832.1:p.Ala1692Thr
NM_001354904.1:c.4999G>A	NP_001341833.1:p.Ala1667Thr
NM_001354904.2:c.4999G>A	NP_001341833.1:p.Ala1667Thr
NM_001354905.1:c.4897G>A	NP_001341834.1:p.Ala1633Thr
NM_001354905.2:c.4897G>A	NP_001341834.1:p.Ala1633Thr
NM_001354906.1:c.4528G>A	NP_001341835.1:p.Ala1510Thr
NM_001354906.2:c.4528G>A	NP_001341835.1:p.Ala1510Thr
ENST00000257430.8:c.5377G>A	ENSP00000257430.4:p.Ala1793Thr
ENST00000504915.3:c.5431G>A	ENSP00000473355.2:p.Ala1811Thr
ENST00000505350.2:c.*5383G>A	ENSP00000481752.1:n.*5383G>A
ENST00000507379.6:c.5323G>A	ENSP00000423224.2:p.Ala1775Thr
ENST00000508376.6:c.5377G>A	ENSP00000427089.2:p.Ala1793Thr
ENST00000508624.5:c.*4699G>A	ENSP00000424265.1:n.*4699G>A
ENST00000509732.6:c.5377G>A	ENSP00000426541.2:p.Ala1793Thr
ENST00000512211.7:c.5377G>A	ENSP00000423828.3:p.Ala1793Thr
ENST00000520401.1:c.230+11999G>A