Canonical Allele Identifier: CA16031358

Gene: APC

Linked Data

• dbSNP Id: rs2149918073
• MyVariant Identifiers: chr5:g.112175870C>A (hg19) ; chr5:g.112840173C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840173C>A , CM000667.2:g.112840173C>A	GRCh38
NC_000005.9:g.112175870C>A , CM000667.1:g.112175870C>A	GRCh37
NC_000005.8:g.112203769C>A	NCBI36
NG_008481.4:g.152653C>A , LRG_130:g.152653C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4633C>A	ENSP00000473355.2:p.Pro1545Thr
ENST00000505350.2:c.*4585C>A	ENSP00000481752.1:n.*4585C>A
ENST00000507379.6:c.4525C>A	ENSP00000423224.2:p.Pro1509Thr
ENST00000509732.6:c.4579C>A	ENSP00000426541.2:p.Pro1527Thr
ENST00000512211.7:c.4579C>A	ENSP00000423828.3:p.Pro1527Thr
ENST00000257430.9:c.4579C>A MANE Select	ENSP00000257430.4:p.Pro1527Thr
ENST00000257430.8:c.4579C>A	ENSP00000257430.4:p.Pro1527Thr
ENST00000508376.6:c.4579C>A	ENSP00000427089.2:p.Pro1527Thr
ENST00000508624.5:c.*3901C>A	ENSP00000424265.1:n.*3901C>A
ENST00000520401.1:c.230+11201C>A
NM_000038.5:c.4579C>A	NP_000029.2:p.Pro1527Thr
NM_001127510.2:c.4579C>A	NP_001120982.1:p.Pro1527Thr
NM_001127511.2:c.4525C>A	NP_001120983.2:p.Pro1509Thr
NM_001354895.1:c.4579C>A	NP_001341824.1:p.Pro1527Thr
NM_001354896.1:c.4633C>A	NP_001341825.1:p.Pro1545Thr
NM_001354897.1:c.4609C>A	NP_001341826.1:p.Pro1537Thr
NM_001354898.1:c.4504C>A	NP_001341827.1:p.Pro1502Thr
NM_001354899.1:c.4495C>A	NP_001341828.1:p.Pro1499Thr
NM_001354900.1:c.4456C>A	NP_001341829.1:p.Pro1486Thr
NM_001354901.1:c.4402C>A	NP_001341830.1:p.Pro1468Thr
NM_001354902.1:c.4306C>A	NP_001341831.1:p.Pro1436Thr
NM_001354903.1:c.4276C>A	NP_001341832.1:p.Pro1426Thr
NM_001354904.1:c.4201C>A	NP_001341833.1:p.Pro1401Thr
NM_001354905.1:c.4099C>A	NP_001341834.1:p.Pro1367Thr
NM_001354906.1:c.3730C>A	NP_001341835.1:p.Pro1244Thr
NM_000038.6:c.4579C>A MANE Select	NP_000029.2:p.Pro1527Thr
NM_001127510.3:c.4579C>A	NP_001120982.1:p.Pro1527Thr
NM_001127511.3:c.4525C>A	NP_001120983.2:p.Pro1509Thr
NM_001354895.2:c.4579C>A	NP_001341824.1:p.Pro1527Thr
NM_001354896.2:c.4633C>A	NP_001341825.1:p.Pro1545Thr
NM_001354897.2:c.4609C>A	NP_001341826.1:p.Pro1537Thr
NM_001354898.2:c.4504C>A	NP_001341827.1:p.Pro1502Thr
NM_001354899.2:c.4495C>A	NP_001341828.1:p.Pro1499Thr
NM_001354900.2:c.4456C>A	NP_001341829.1:p.Pro1486Thr
NM_001354901.2:c.4402C>A	NP_001341830.1:p.Pro1468Thr
NM_001354902.2:c.4306C>A	NP_001341831.1:p.Pro1436Thr
NM_001354903.2:c.4276C>A	NP_001341832.1:p.Pro1426Thr
NM_001354904.2:c.4201C>A	NP_001341833.1:p.Pro1401Thr
NM_001354905.2:c.4099C>A	NP_001341834.1:p.Pro1367Thr
NM_001354906.2:c.3730C>A	NP_001341835.1:p.Pro1244Thr