Canonical Allele Identifier: CA16030960

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839990G>T , CM000667.2:g.112839990G>T	GRCh38
NC_000005.9:g.112175687G>T , CM000667.1:g.112175687G>T	GRCh37
NC_000005.8:g.112203586G>T	NCBI36
NG_008481.4:g.152470G>T , LRG_130:g.152470G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.4396G>T MANE Select	NP_000029.2:p.Gly1466Ter
ENST00000257430.9:c.4396G>T MANE Select	ENSP00000257430.4:p.Gly1466Ter
NM_000038.5:c.4396G>T	NP_000029.2:p.Gly1466Ter
NM_001127510.2:c.4396G>T	NP_001120982.1:p.Gly1466Ter
NM_001127510.3:c.4396G>T	NP_001120982.1:p.Gly1466Ter
NM_001127511.2:c.4342G>T	NP_001120983.2:p.Gly1448Ter
NM_001127511.3:c.4342G>T	NP_001120983.2:p.Gly1448Ter
NM_001354895.1:c.4396G>T	NP_001341824.1:p.Gly1466Ter
NM_001354895.2:c.4396G>T	NP_001341824.1:p.Gly1466Ter
NM_001354896.1:c.4450G>T	NP_001341825.1:p.Gly1484Ter
NM_001354896.2:c.4450G>T	NP_001341825.1:p.Gly1484Ter
NM_001354897.1:c.4426G>T	NP_001341826.1:p.Gly1476Ter
NM_001354897.2:c.4426G>T	NP_001341826.1:p.Gly1476Ter
NM_001354898.1:c.4321G>T	NP_001341827.1:p.Gly1441Ter
NM_001354898.2:c.4321G>T	NP_001341827.1:p.Gly1441Ter
NM_001354899.1:c.4312G>T	NP_001341828.1:p.Gly1438Ter
NM_001354899.2:c.4312G>T	NP_001341828.1:p.Gly1438Ter
NM_001354900.1:c.4273G>T	NP_001341829.1:p.Gly1425Ter
NM_001354900.2:c.4273G>T	NP_001341829.1:p.Gly1425Ter
NM_001354901.1:c.4219G>T	NP_001341830.1:p.Gly1407Ter
NM_001354901.2:c.4219G>T	NP_001341830.1:p.Gly1407Ter
NM_001354902.1:c.4123G>T	NP_001341831.1:p.Gly1375Ter
NM_001354902.2:c.4123G>T	NP_001341831.1:p.Gly1375Ter
NM_001354903.1:c.4093G>T	NP_001341832.1:p.Gly1365Ter
NM_001354903.2:c.4093G>T	NP_001341832.1:p.Gly1365Ter
NM_001354904.1:c.4018G>T	NP_001341833.1:p.Gly1340Ter
NM_001354904.2:c.4018G>T	NP_001341833.1:p.Gly1340Ter
NM_001354905.1:c.3916G>T	NP_001341834.1:p.Gly1306Ter
NM_001354905.2:c.3916G>T	NP_001341834.1:p.Gly1306Ter
NM_001354906.1:c.3547G>T	NP_001341835.1:p.Gly1183Ter
NM_001354906.2:c.3547G>T	NP_001341835.1:p.Gly1183Ter
ENST00000257430.8:c.4396G>T	ENSP00000257430.4:p.Gly1466Ter
ENST00000504915.3:c.4450G>T	ENSP00000473355.2:p.Gly1484Ter
ENST00000505350.2:c.*4402G>T	ENSP00000481752.1:n.*4402G>T
ENST00000507379.6:c.4342G>T	ENSP00000423224.2:p.Gly1448Ter
ENST00000508376.6:c.4396G>T	ENSP00000427089.2:p.Gly1466Ter
ENST00000508624.5:c.*3718G>T	ENSP00000424265.1:n.*3718G>T
ENST00000509732.6:c.4396G>T	ENSP00000426541.2:p.Gly1466Ter
ENST00000512211.7:c.4396G>T	ENSP00000423828.3:p.Gly1466Ter
ENST00000520401.1:c.230+11018G>T