Canonical Allele Identifier: CA16031355

Gene: APC

Linked Data

• dbSNP Id: rs1325776789
• MyVariant Identifiers: chr5:g.112175868C>A (hg19) ; chr5:g.112840171C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840171C>A , CM000667.2:g.112840171C>A	GRCh38
NC_000005.9:g.112175868C>A , CM000667.1:g.112175868C>A	GRCh37
NC_000005.8:g.112203767C>A	NCBI36
NG_008481.4:g.152651C>A , LRG_130:g.152651C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.4631C>A	ENSP00000473355.2:p.Pro1544His
ENST00000505350.2:c.*4583C>A	ENSP00000481752.1:n.*4583C>A
ENST00000507379.6:c.4523C>A	ENSP00000423224.2:p.Pro1508His
ENST00000509732.6:c.4577C>A	ENSP00000426541.2:p.Pro1526His
ENST00000512211.7:c.4577C>A	ENSP00000423828.3:p.Pro1526His
ENST00000257430.9:c.4577C>A MANE Select	ENSP00000257430.4:p.Pro1526His
ENST00000257430.8:c.4577C>A	ENSP00000257430.4:p.Pro1526His
ENST00000508376.6:c.4577C>A	ENSP00000427089.2:p.Pro1526His
ENST00000508624.5:c.*3899C>A	ENSP00000424265.1:n.*3899C>A
ENST00000520401.1:c.230+11199C>A
NM_000038.5:c.4577C>A	NP_000029.2:p.Pro1526His
NM_001127510.2:c.4577C>A	NP_001120982.1:p.Pro1526His
NM_001127511.2:c.4523C>A	NP_001120983.2:p.Pro1508His
NM_001354895.1:c.4577C>A	NP_001341824.1:p.Pro1526His
NM_001354896.1:c.4631C>A	NP_001341825.1:p.Pro1544His
NM_001354897.1:c.4607C>A	NP_001341826.1:p.Pro1536His
NM_001354898.1:c.4502C>A	NP_001341827.1:p.Pro1501His
NM_001354899.1:c.4493C>A	NP_001341828.1:p.Pro1498His
NM_001354900.1:c.4454C>A	NP_001341829.1:p.Pro1485His
NM_001354901.1:c.4400C>A	NP_001341830.1:p.Pro1467His
NM_001354902.1:c.4304C>A	NP_001341831.1:p.Pro1435His
NM_001354903.1:c.4274C>A	NP_001341832.1:p.Pro1425His
NM_001354904.1:c.4199C>A	NP_001341833.1:p.Pro1400His
NM_001354905.1:c.4097C>A	NP_001341834.1:p.Pro1366His
NM_001354906.1:c.3728C>A	NP_001341835.1:p.Pro1243His
NM_000038.6:c.4577C>A MANE Select	NP_000029.2:p.Pro1526His
NM_001127510.3:c.4577C>A	NP_001120982.1:p.Pro1526His
NM_001127511.3:c.4523C>A	NP_001120983.2:p.Pro1508His
NM_001354895.2:c.4577C>A	NP_001341824.1:p.Pro1526His
NM_001354896.2:c.4631C>A	NP_001341825.1:p.Pro1544His
NM_001354897.2:c.4607C>A	NP_001341826.1:p.Pro1536His
NM_001354898.2:c.4502C>A	NP_001341827.1:p.Pro1501His
NM_001354899.2:c.4493C>A	NP_001341828.1:p.Pro1498His
NM_001354900.2:c.4454C>A	NP_001341829.1:p.Pro1485His
NM_001354901.2:c.4400C>A	NP_001341830.1:p.Pro1467His
NM_001354902.2:c.4304C>A	NP_001341831.1:p.Pro1435His
NM_001354903.2:c.4274C>A	NP_001341832.1:p.Pro1425His
NM_001354904.2:c.4199C>A	NP_001341833.1:p.Pro1400His
NM_001354905.2:c.4097C>A	NP_001341834.1:p.Pro1366His
NM_001354906.2:c.3728C>A	NP_001341835.1:p.Pro1243His