Canonical Allele Identifier: CA16024323

Gene: APC

Linked Data

• ClinVar Variation Id: 2584095
• ClinVar RCV Id: RCV003337641
• COSMIC: COSM4169479
• MyVariant Identifiers: chr5:g.112157658G>T (hg19) ; chr5:g.112821961G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112821961G>T , CM000667.2:g.112821961G>T	GRCh38
NC_000005.9:g.112157658G>T , CM000667.1:g.112157658G>T	GRCh37
NC_000005.8:g.112185557G>T	NCBI36
NG_008481.4:g.134441G>T , LRG_130:g.134441G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1378G>T	ENSP00000484935.2:p.Glu460Ter
ENST00000504915.3:c.1378G>T	ENSP00000473355.2:p.Glu460Ter
ENST00000505084.2:n.1434G>T
ENST00000505350.2:c.*1384G>T	ENSP00000481752.1:n.*1384G>T
ENST00000507379.6:c.1324G>T	ENSP00000423224.2:p.Glu442Ter
ENST00000509732.6:c.1378G>T	ENSP00000426541.2:p.Glu460Ter
ENST00000512211.7:c.1378G>T	ENSP00000423828.3:p.Glu460Ter
ENST00000257430.9:c.1378G>T MANE Select	ENSP00000257430.4:p.Glu460Ter
ENST00000257430.8:c.1378G>T	ENSP00000257430.4:p.Glu460Ter
ENST00000502371.2:c.66G>T
ENST00000504915.2:c.13G>T	ENSP00000473355.1:p.Glu5Ter
ENST00000507379.5:c.1324G>T	ENSP00000423224.1:p.Glu442Ter
ENST00000508376.6:c.1378G>T	ENSP00000427089.2:p.Glu460Ter
ENST00000508624.5:c.*700G>T	ENSP00000424265.1:n.*700G>T
ENST00000512211.6:c.1378G>T	ENSP00000423828.2:p.Glu460Ter
NM_000038.5:c.1378G>T	NP_000029.2:p.Glu460Ter
NM_001127510.2:c.1378G>T	NP_001120982.1:p.Glu460Ter
NM_001127511.2:c.1324G>T	NP_001120983.2:p.Glu442Ter
NM_001354895.1:c.1378G>T	NP_001341824.1:p.Glu460Ter
NM_001354896.1:c.1378G>T	NP_001341825.1:p.Glu460Ter
NM_001354897.1:c.1408G>T	NP_001341826.1:p.Glu470Ter
NM_001354898.1:c.1303G>T	NP_001341827.1:p.Glu435Ter
NM_001354899.1:c.1294G>T	NP_001341828.1:p.Glu432Ter
NM_001354900.1:c.1201G>T	NP_001341829.1:p.Glu401Ter
NM_001354901.1:c.1201G>T	NP_001341830.1:p.Glu401Ter
NM_001354902.1:c.1105G>T	NP_001341831.1:p.Glu369Ter
NM_001354903.1:c.1075G>T	NP_001341832.1:p.Glu359Ter
NM_001354904.1:c.1000G>T	NP_001341833.1:p.Glu334Ter
NM_001354905.1:c.898G>T	NP_001341834.1:p.Glu300Ter
NM_001354906.1:c.529G>T	NP_001341835.1:p.Glu177Ter
NM_000038.6:c.1378G>T MANE Select	NP_000029.2:p.Glu460Ter
NM_001127510.3:c.1378G>T	NP_001120982.1:p.Glu460Ter
NM_001127511.3:c.1324G>T	NP_001120983.2:p.Glu442Ter
NM_001354895.2:c.1378G>T	NP_001341824.1:p.Glu460Ter
NM_001354896.2:c.1378G>T	NP_001341825.1:p.Glu460Ter
NM_001354897.2:c.1408G>T	NP_001341826.1:p.Glu470Ter
NM_001354898.2:c.1303G>T	NP_001341827.1:p.Glu435Ter
NM_001354899.2:c.1294G>T	NP_001341828.1:p.Glu432Ter
NM_001354900.2:c.1201G>T	NP_001341829.1:p.Glu401Ter
NM_001354901.2:c.1201G>T	NP_001341830.1:p.Glu401Ter
NM_001354902.2:c.1105G>T	NP_001341831.1:p.Glu369Ter
NM_001354903.2:c.1075G>T	NP_001341832.1:p.Glu359Ter
NM_001354904.2:c.1000G>T	NP_001341833.1:p.Glu334Ter
NM_001354905.2:c.898G>T	NP_001341834.1:p.Glu300Ter
NM_001354906.2:c.529G>T	NP_001341835.1:p.Glu177Ter