Canonical Allele Identifier: CA16024934

Gene: APC

Linked Data

• dbSNP Id: rs398123116
• MyVariant Identifiers: chr5:g.112164585G>C (hg19) ; chr5:g.112828888G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828888G>C , CM000667.2:g.112828888G>C	GRCh38
NC_000005.9:g.112164585G>C , CM000667.1:g.112164585G>C	GRCh37
NC_000005.8:g.112192484G>C	NCBI36
NG_008481.4:g.141368G>C , LRG_130:g.141368G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1409-6063G>C	ENSP00000484935.2:n.1409-6063G>C
ENST00000504915.3:c.1713G>C	ENSP00000473355.2:p.Trp571Cys
ENST00000505084.2:n.1715G>C
ENST00000505350.2:c.*1665G>C	ENSP00000481752.1:n.*1665G>C
ENST00000507379.6:c.1605G>C	ENSP00000423224.2:p.Trp535Cys
ENST00000509732.6:c.1659G>C	ENSP00000426541.2:p.Trp553Cys
ENST00000512211.7:c.1659G>C	ENSP00000423828.3:p.Trp553Cys
ENST00000257430.9:c.1659G>C MANE Select	ENSP00000257430.4:p.Trp553Cys
ENST00000257430.8:c.1659G>C	ENSP00000257430.4:p.Trp553Cys
ENST00000502371.2:c.97-6063G>C
ENST00000504915.2:c.348G>C	ENSP00000473355.1:p.Trp116Cys
ENST00000505084.1:n.146G>C
ENST00000507379.5:c.1605G>C	ENSP00000423224.1:p.Trp535Cys
ENST00000508376.6:c.1659G>C	ENSP00000427089.2:p.Trp553Cys
ENST00000508624.5:c.*981G>C	ENSP00000424265.1:n.*981G>C
ENST00000512211.6:c.1659G>C	ENSP00000423828.2:p.Trp553Cys
ENST00000520401.1:c.146G>C
NM_000038.5:c.1659G>C	NP_000029.2:p.Trp553Cys
NM_001127510.2:c.1659G>C	NP_001120982.1:p.Trp553Cys
NM_001127511.2:c.1605G>C	NP_001120983.2:p.Trp535Cys
NM_001354895.1:c.1659G>C	NP_001341824.1:p.Trp553Cys
NM_001354896.1:c.1713G>C	NP_001341825.1:p.Trp571Cys
NM_001354897.1:c.1689G>C	NP_001341826.1:p.Trp563Cys
NM_001354898.1:c.1584G>C	NP_001341827.1:p.Trp528Cys
NM_001354899.1:c.1575G>C	NP_001341828.1:p.Trp525Cys
NM_001354900.1:c.1536G>C	NP_001341829.1:p.Trp512Cys
NM_001354901.1:c.1482G>C	NP_001341830.1:p.Trp494Cys
NM_001354902.1:c.1386G>C	NP_001341831.1:p.Trp462Cys
NM_001354903.1:c.1356G>C	NP_001341832.1:p.Trp452Cys
NM_001354904.1:c.1281G>C	NP_001341833.1:p.Trp427Cys
NM_001354905.1:c.1179G>C	NP_001341834.1:p.Trp393Cys
NM_001354906.1:c.810G>C	NP_001341835.1:p.Trp270Cys
NM_000038.6:c.1659G>C MANE Select	NP_000029.2:p.Trp553Cys
NM_001127510.3:c.1659G>C	NP_001120982.1:p.Trp553Cys
NM_001127511.3:c.1605G>C	NP_001120983.2:p.Trp535Cys
NM_001354895.2:c.1659G>C	NP_001341824.1:p.Trp553Cys
NM_001354896.2:c.1713G>C	NP_001341825.1:p.Trp571Cys
NM_001354897.2:c.1689G>C	NP_001341826.1:p.Trp563Cys
NM_001354898.2:c.1584G>C	NP_001341827.1:p.Trp528Cys
NM_001354899.2:c.1575G>C	NP_001341828.1:p.Trp525Cys
NM_001354900.2:c.1536G>C	NP_001341829.1:p.Trp512Cys
NM_001354901.2:c.1482G>C	NP_001341830.1:p.Trp494Cys
NM_001354902.2:c.1386G>C	NP_001341831.1:p.Trp462Cys
NM_001354903.2:c.1356G>C	NP_001341832.1:p.Trp452Cys
NM_001354904.2:c.1281G>C	NP_001341833.1:p.Trp427Cys
NM_001354905.2:c.1179G>C	NP_001341834.1:p.Trp393Cys
NM_001354906.2:c.810G>C	NP_001341835.1:p.Trp270Cys