Canonical Allele Identifier: CA16031488

Gene: APC

Linked Data

• dbSNP Id: rs1554086031
• MyVariant Identifiers: chr5:g.112175927A>G (hg19) ; chr5:g.112840230A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840230A>G , CM000667.2:g.112840230A>G	GRCh38
NC_000005.9:g.112175927A>G , CM000667.1:g.112175927A>G	GRCh37
NC_000005.8:g.112203826A>G	NCBI36
NG_008481.4:g.152710A>G , LRG_130:g.152710A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4690A>G	ENSP00000473355.2:p.Asn1564Asp
ENST00000505350.2:c.*4642A>G	ENSP00000481752.1:n.*4642A>G
ENST00000507379.6:c.4582A>G	ENSP00000423224.2:p.Asn1528Asp
ENST00000509732.6:c.4636A>G	ENSP00000426541.2:p.Asn1546Asp
ENST00000512211.7:c.4636A>G	ENSP00000423828.3:p.Asn1546Asp
ENST00000257430.9:c.4636A>G MANE Select	ENSP00000257430.4:p.Asn1546Asp
ENST00000257430.8:c.4636A>G	ENSP00000257430.4:p.Asn1546Asp
ENST00000508376.6:c.4636A>G	ENSP00000427089.2:p.Asn1546Asp
ENST00000508624.5:c.*3958A>G	ENSP00000424265.1:n.*3958A>G
ENST00000520401.1:c.230+11258A>G
NM_000038.5:c.4636A>G	NP_000029.2:p.Asn1546Asp
NM_001127510.2:c.4636A>G	NP_001120982.1:p.Asn1546Asp
NM_001127511.2:c.4582A>G	NP_001120983.2:p.Asn1528Asp
NM_001354895.1:c.4636A>G	NP_001341824.1:p.Asn1546Asp
NM_001354896.1:c.4690A>G	NP_001341825.1:p.Asn1564Asp
NM_001354897.1:c.4666A>G	NP_001341826.1:p.Asn1556Asp
NM_001354898.1:c.4561A>G	NP_001341827.1:p.Asn1521Asp
NM_001354899.1:c.4552A>G	NP_001341828.1:p.Asn1518Asp
NM_001354900.1:c.4513A>G	NP_001341829.1:p.Asn1505Asp
NM_001354901.1:c.4459A>G	NP_001341830.1:p.Asn1487Asp
NM_001354902.1:c.4363A>G	NP_001341831.1:p.Asn1455Asp
NM_001354903.1:c.4333A>G	NP_001341832.1:p.Asn1445Asp
NM_001354904.1:c.4258A>G	NP_001341833.1:p.Asn1420Asp
NM_001354905.1:c.4156A>G	NP_001341834.1:p.Asn1386Asp
NM_001354906.1:c.3787A>G	NP_001341835.1:p.Asn1263Asp
NM_000038.6:c.4636A>G MANE Select	NP_000029.2:p.Asn1546Asp
NM_001127510.3:c.4636A>G	NP_001120982.1:p.Asn1546Asp
NM_001127511.3:c.4582A>G	NP_001120983.2:p.Asn1528Asp
NM_001354895.2:c.4636A>G	NP_001341824.1:p.Asn1546Asp
NM_001354896.2:c.4690A>G	NP_001341825.1:p.Asn1564Asp
NM_001354897.2:c.4666A>G	NP_001341826.1:p.Asn1556Asp
NM_001354898.2:c.4561A>G	NP_001341827.1:p.Asn1521Asp
NM_001354899.2:c.4552A>G	NP_001341828.1:p.Asn1518Asp
NM_001354900.2:c.4513A>G	NP_001341829.1:p.Asn1505Asp
NM_001354901.2:c.4459A>G	NP_001341830.1:p.Asn1487Asp
NM_001354902.2:c.4363A>G	NP_001341831.1:p.Asn1455Asp
NM_001354903.2:c.4333A>G	NP_001341832.1:p.Asn1445Asp
NM_001354904.2:c.4258A>G	NP_001341833.1:p.Asn1420Asp
NM_001354905.2:c.4156A>G	NP_001341834.1:p.Asn1386Asp
NM_001354906.2:c.3787A>G	NP_001341835.1:p.Asn1263Asp