Canonical Allele Identifier: CA16023927

Gene: APC

Linked Data

• dbSNP Id: rs786202331
• MyVariant Identifiers: chr5:g.112154926A>T (hg19) ; chr5:g.112819229A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112819229A>T , CM000667.2:g.112819229A>T	GRCh38
NC_000005.9:g.112154926A>T , CM000667.1:g.112154926A>T	GRCh37
NC_000005.8:g.112182825A>T	NCBI36
NG_008481.4:g.131709A>T , LRG_130:g.131709A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1197A>T	ENSP00000484935.2:p.Arg399Ser
ENST00000504915.3:c.1197A>T	ENSP00000473355.2:p.Arg399Ser
ENST00000505084.2:n.1253A>T
ENST00000505350.2:c.*1203A>T	ENSP00000481752.1:n.*1203A>T
ENST00000507379.6:c.1143A>T	ENSP00000423224.2:p.Arg381Ser
ENST00000509732.6:c.1197A>T	ENSP00000426541.2:p.Arg399Ser
ENST00000512211.7:c.1197A>T	ENSP00000423828.3:p.Arg399Ser
ENST00000257430.9:c.1197A>T MANE Select	ENSP00000257430.4:p.Arg399Ser
ENST00000257430.8:c.1197A>T	ENSP00000257430.4:p.Arg399Ser
ENST00000507379.5:c.1143A>T	ENSP00000423224.1:p.Arg381Ser
ENST00000508376.6:c.1197A>T	ENSP00000427089.2:p.Arg399Ser
ENST00000508624.5:c.*519A>T	ENSP00000424265.1:n.*519A>T
ENST00000512211.6:c.1197A>T	ENSP00000423828.2:p.Arg399Ser
NM_000038.5:c.1197A>T	NP_000029.2:p.Arg399Ser
NM_001127510.2:c.1197A>T	NP_001120982.1:p.Arg399Ser
NM_001127511.2:c.1143A>T	NP_001120983.2:p.Arg381Ser
NM_001354895.1:c.1197A>T	NP_001341824.1:p.Arg399Ser
NM_001354896.1:c.1197A>T	NP_001341825.1:p.Arg399Ser
NM_001354897.1:c.1227A>T	NP_001341826.1:p.Arg409Ser
NM_001354898.1:c.1122A>T	NP_001341827.1:p.Arg374Ser
NM_001354899.1:c.1113A>T	NP_001341828.1:p.Arg371Ser
NM_001354900.1:c.1020A>T	NP_001341829.1:p.Arg340Ser
NM_001354901.1:c.1020A>T	NP_001341830.1:p.Arg340Ser
NM_001354902.1:c.964-40A>T	NP_001341831.1:n.964-40A>T
NM_001354903.1:c.934-40A>T	NP_001341832.1:n.934-40A>T
NM_001354904.1:c.859-40A>T	NP_001341833.1:n.859-40A>T
NM_001354905.1:c.757-40A>T	NP_001341834.1:n.757-40A>T
NM_001354906.1:c.348A>T	NP_001341835.1:p.Arg116Ser
NM_000038.6:c.1197A>T MANE Select	NP_000029.2:p.Arg399Ser
NM_001127510.3:c.1197A>T	NP_001120982.1:p.Arg399Ser
NM_001127511.3:c.1143A>T	NP_001120983.2:p.Arg381Ser
NM_001354895.2:c.1197A>T	NP_001341824.1:p.Arg399Ser
NM_001354896.2:c.1197A>T	NP_001341825.1:p.Arg399Ser
NM_001354897.2:c.1227A>T	NP_001341826.1:p.Arg409Ser
NM_001354898.2:c.1122A>T	NP_001341827.1:p.Arg374Ser
NM_001354899.2:c.1113A>T	NP_001341828.1:p.Arg371Ser
NM_001354900.2:c.1020A>T	NP_001341829.1:p.Arg340Ser
NM_001354901.2:c.1020A>T	NP_001341830.1:p.Arg340Ser
NM_001354902.2:c.964-40A>T	NP_001341831.1:n.964-40A>T
NM_001354903.2:c.934-40A>T	NP_001341832.1:n.934-40A>T
NM_001354904.2:c.859-40A>T	NP_001341833.1:n.859-40A>T
NM_001354905.2:c.757-40A>T	NP_001341834.1:n.757-40A>T
NM_001354906.2:c.348A>T	NP_001341835.1:p.Arg116Ser