Canonical Allele Identifier: CA16031634

Gene: APC

Linked Data

• dbSNP Id: rs2149921486
• MyVariant Identifiers: chr5:g.112175990T>A (hg19) ; chr5:g.112840293T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840293T>A , CM000667.2:g.112840293T>A	GRCh38
NC_000005.9:g.112175990T>A , CM000667.1:g.112175990T>A	GRCh37
NC_000005.8:g.112203889T>A	NCBI36
NG_008481.4:g.152773T>A , LRG_130:g.152773T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4753T>A	ENSP00000473355.2:p.Ser1585Thr
ENST00000505350.2:c.*4705T>A	ENSP00000481752.1:n.*4705T>A
ENST00000507379.6:c.4645T>A	ENSP00000423224.2:p.Ser1549Thr
ENST00000509732.6:c.4699T>A	ENSP00000426541.2:p.Ser1567Thr
ENST00000512211.7:c.4699T>A	ENSP00000423828.3:p.Ser1567Thr
ENST00000257430.9:c.4699T>A MANE Select	ENSP00000257430.4:p.Ser1567Thr
ENST00000257430.8:c.4699T>A	ENSP00000257430.4:p.Ser1567Thr
ENST00000508376.6:c.4699T>A	ENSP00000427089.2:p.Ser1567Thr
ENST00000508624.5:c.*4021T>A	ENSP00000424265.1:n.*4021T>A
ENST00000520401.1:c.230+11321T>A
NM_000038.5:c.4699T>A	NP_000029.2:p.Ser1567Thr
NM_001127510.2:c.4699T>A	NP_001120982.1:p.Ser1567Thr
NM_001127511.2:c.4645T>A	NP_001120983.2:p.Ser1549Thr
NM_001354895.1:c.4699T>A	NP_001341824.1:p.Ser1567Thr
NM_001354896.1:c.4753T>A	NP_001341825.1:p.Ser1585Thr
NM_001354897.1:c.4729T>A	NP_001341826.1:p.Ser1577Thr
NM_001354898.1:c.4624T>A	NP_001341827.1:p.Ser1542Thr
NM_001354899.1:c.4615T>A	NP_001341828.1:p.Ser1539Thr
NM_001354900.1:c.4576T>A	NP_001341829.1:p.Ser1526Thr
NM_001354901.1:c.4522T>A	NP_001341830.1:p.Ser1508Thr
NM_001354902.1:c.4426T>A	NP_001341831.1:p.Ser1476Thr
NM_001354903.1:c.4396T>A	NP_001341832.1:p.Ser1466Thr
NM_001354904.1:c.4321T>A	NP_001341833.1:p.Ser1441Thr
NM_001354905.1:c.4219T>A	NP_001341834.1:p.Ser1407Thr
NM_001354906.1:c.3850T>A	NP_001341835.1:p.Ser1284Thr
NM_000038.6:c.4699T>A MANE Select	NP_000029.2:p.Ser1567Thr
NM_001127510.3:c.4699T>A	NP_001120982.1:p.Ser1567Thr
NM_001127511.3:c.4645T>A	NP_001120983.2:p.Ser1549Thr
NM_001354895.2:c.4699T>A	NP_001341824.1:p.Ser1567Thr
NM_001354896.2:c.4753T>A	NP_001341825.1:p.Ser1585Thr
NM_001354897.2:c.4729T>A	NP_001341826.1:p.Ser1577Thr
NM_001354898.2:c.4624T>A	NP_001341827.1:p.Ser1542Thr
NM_001354899.2:c.4615T>A	NP_001341828.1:p.Ser1539Thr
NM_001354900.2:c.4576T>A	NP_001341829.1:p.Ser1526Thr
NM_001354901.2:c.4522T>A	NP_001341830.1:p.Ser1508Thr
NM_001354902.2:c.4426T>A	NP_001341831.1:p.Ser1476Thr
NM_001354903.2:c.4396T>A	NP_001341832.1:p.Ser1466Thr
NM_001354904.2:c.4321T>A	NP_001341833.1:p.Ser1441Thr
NM_001354905.2:c.4219T>A	NP_001341834.1:p.Ser1407Thr
NM_001354906.2:c.3850T>A	NP_001341835.1:p.Ser1284Thr