Canonical Allele Identifier: CA16024327

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112157660A>C (hg19) ; chr5:g.112821963A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112821963A>C , CM000667.2:g.112821963A>C	GRCh38
NC_000005.9:g.112157660A>C , CM000667.1:g.112157660A>C	GRCh37
NC_000005.8:g.112185559A>C	NCBI36
NG_008481.4:g.134443A>C , LRG_130:g.134443A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1380A>C	ENSP00000484935.2:p.Glu460Asp
ENST00000504915.3:c.1380A>C	ENSP00000473355.2:p.Glu460Asp
ENST00000505084.2:n.1436A>C
ENST00000505350.2:c.*1386A>C	ENSP00000481752.1:n.*1386A>C
ENST00000507379.6:c.1326A>C	ENSP00000423224.2:p.Glu442Asp
ENST00000509732.6:c.1380A>C	ENSP00000426541.2:p.Glu460Asp
ENST00000512211.7:c.1380A>C	ENSP00000423828.3:p.Glu460Asp
ENST00000257430.9:c.1380A>C MANE Select	ENSP00000257430.4:p.Glu460Asp
ENST00000257430.8:c.1380A>C	ENSP00000257430.4:p.Glu460Asp
ENST00000502371.2:c.68A>C
ENST00000504915.2:c.15A>C	ENSP00000473355.1:p.Glu5Asp
ENST00000507379.5:c.1326A>C	ENSP00000423224.1:p.Glu442Asp
ENST00000508376.6:c.1380A>C	ENSP00000427089.2:p.Glu460Asp
ENST00000508624.5:c.*702A>C	ENSP00000424265.1:n.*702A>C
ENST00000512211.6:c.1380A>C	ENSP00000423828.2:p.Glu460Asp
NM_000038.5:c.1380A>C	NP_000029.2:p.Glu460Asp
NM_001127510.2:c.1380A>C	NP_001120982.1:p.Glu460Asp
NM_001127511.2:c.1326A>C	NP_001120983.2:p.Glu442Asp
NM_001354895.1:c.1380A>C	NP_001341824.1:p.Glu460Asp
NM_001354896.1:c.1380A>C	NP_001341825.1:p.Glu460Asp
NM_001354897.1:c.1410A>C	NP_001341826.1:p.Glu470Asp
NM_001354898.1:c.1305A>C	NP_001341827.1:p.Glu435Asp
NM_001354899.1:c.1296A>C	NP_001341828.1:p.Glu432Asp
NM_001354900.1:c.1203A>C	NP_001341829.1:p.Glu401Asp
NM_001354901.1:c.1203A>C	NP_001341830.1:p.Glu401Asp
NM_001354902.1:c.1107A>C	NP_001341831.1:p.Glu369Asp
NM_001354903.1:c.1077A>C	NP_001341832.1:p.Glu359Asp
NM_001354904.1:c.1002A>C	NP_001341833.1:p.Glu334Asp
NM_001354905.1:c.900A>C	NP_001341834.1:p.Glu300Asp
NM_001354906.1:c.531A>C	NP_001341835.1:p.Glu177Asp
NM_000038.6:c.1380A>C MANE Select	NP_000029.2:p.Glu460Asp
NM_001127510.3:c.1380A>C	NP_001120982.1:p.Glu460Asp
NM_001127511.3:c.1326A>C	NP_001120983.2:p.Glu442Asp
NM_001354895.2:c.1380A>C	NP_001341824.1:p.Glu460Asp
NM_001354896.2:c.1380A>C	NP_001341825.1:p.Glu460Asp
NM_001354897.2:c.1410A>C	NP_001341826.1:p.Glu470Asp
NM_001354898.2:c.1305A>C	NP_001341827.1:p.Glu435Asp
NM_001354899.2:c.1296A>C	NP_001341828.1:p.Glu432Asp
NM_001354900.2:c.1203A>C	NP_001341829.1:p.Glu401Asp
NM_001354901.2:c.1203A>C	NP_001341830.1:p.Glu401Asp
NM_001354902.2:c.1107A>C	NP_001341831.1:p.Glu369Asp
NM_001354903.2:c.1077A>C	NP_001341832.1:p.Glu359Asp
NM_001354904.2:c.1002A>C	NP_001341833.1:p.Glu334Asp
NM_001354905.2:c.900A>C	NP_001341834.1:p.Glu300Asp
NM_001354906.2:c.531A>C	NP_001341835.1:p.Glu177Asp