Canonical Allele Identifier: CA16032578

Gene: APC

Linked Data

• dbSNP Id: rs1765858509
• MyVariant Identifiers: chr5:g.112176437A>T (hg19) ; chr5:g.112840740A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840740A>T , CM000667.2:g.112840740A>T	GRCh38
NC_000005.9:g.112176437A>T , CM000667.1:g.112176437A>T	GRCh37
NC_000005.8:g.112204336A>T	NCBI36
NG_008481.4:g.153220A>T , LRG_130:g.153220A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.5200A>T	ENSP00000473355.2:p.Asn1734Tyr
ENST00000505350.2:c.*5152A>T	ENSP00000481752.1:n.*5152A>T
ENST00000507379.6:c.5092A>T	ENSP00000423224.2:p.Asn1698Tyr
ENST00000509732.6:c.5146A>T	ENSP00000426541.2:p.Asn1716Tyr
ENST00000512211.7:c.5146A>T	ENSP00000423828.3:p.Asn1716Tyr
ENST00000257430.9:c.5146A>T MANE Select	ENSP00000257430.4:p.Asn1716Tyr
ENST00000257430.8:c.5146A>T	ENSP00000257430.4:p.Asn1716Tyr
ENST00000508376.6:c.5146A>T	ENSP00000427089.2:p.Asn1716Tyr
ENST00000508624.5:c.*4468A>T	ENSP00000424265.1:n.*4468A>T
ENST00000520401.1:c.230+11768A>T
NM_000038.5:c.5146A>T	NP_000029.2:p.Asn1716Tyr
NM_001127510.2:c.5146A>T	NP_001120982.1:p.Asn1716Tyr
NM_001127511.2:c.5092A>T	NP_001120983.2:p.Asn1698Tyr
NM_001354895.1:c.5146A>T	NP_001341824.1:p.Asn1716Tyr
NM_001354896.1:c.5200A>T	NP_001341825.1:p.Asn1734Tyr
NM_001354897.1:c.5176A>T	NP_001341826.1:p.Asn1726Tyr
NM_001354898.1:c.5071A>T	NP_001341827.1:p.Asn1691Tyr
NM_001354899.1:c.5062A>T	NP_001341828.1:p.Asn1688Tyr
NM_001354900.1:c.5023A>T	NP_001341829.1:p.Asn1675Tyr
NM_001354901.1:c.4969A>T	NP_001341830.1:p.Asn1657Tyr
NM_001354902.1:c.4873A>T	NP_001341831.1:p.Asn1625Tyr
NM_001354903.1:c.4843A>T	NP_001341832.1:p.Asn1615Tyr
NM_001354904.1:c.4768A>T	NP_001341833.1:p.Asn1590Tyr
NM_001354905.1:c.4666A>T	NP_001341834.1:p.Asn1556Tyr
NM_001354906.1:c.4297A>T	NP_001341835.1:p.Asn1433Tyr
NM_000038.6:c.5146A>T MANE Select	NP_000029.2:p.Asn1716Tyr
NM_001127510.3:c.5146A>T	NP_001120982.1:p.Asn1716Tyr
NM_001127511.3:c.5092A>T	NP_001120983.2:p.Asn1698Tyr
NM_001354895.2:c.5146A>T	NP_001341824.1:p.Asn1716Tyr
NM_001354896.2:c.5200A>T	NP_001341825.1:p.Asn1734Tyr
NM_001354897.2:c.5176A>T	NP_001341826.1:p.Asn1726Tyr
NM_001354898.2:c.5071A>T	NP_001341827.1:p.Asn1691Tyr
NM_001354899.2:c.5062A>T	NP_001341828.1:p.Asn1688Tyr
NM_001354900.2:c.5023A>T	NP_001341829.1:p.Asn1675Tyr
NM_001354901.2:c.4969A>T	NP_001341830.1:p.Asn1657Tyr
NM_001354902.2:c.4873A>T	NP_001341831.1:p.Asn1625Tyr
NM_001354903.2:c.4843A>T	NP_001341832.1:p.Asn1615Tyr
NM_001354904.2:c.4768A>T	NP_001341833.1:p.Asn1590Tyr
NM_001354905.2:c.4666A>T	NP_001341834.1:p.Asn1556Tyr
NM_001354906.2:c.4297A>T	NP_001341835.1:p.Asn1433Tyr