Canonical Allele Identifier: CA16024930

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112164583T>C (hg19) ; chr5:g.112828886T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828886T>C , CM000667.2:g.112828886T>C	GRCh38
NC_000005.9:g.112164583T>C , CM000667.1:g.112164583T>C	GRCh37
NC_000005.8:g.112192482T>C	NCBI36
NG_008481.4:g.141366T>C , LRG_130:g.141366T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1409-6065T>C	ENSP00000484935.2:n.1409-6065T>C
ENST00000504915.3:c.1711T>C	ENSP00000473355.2:p.Trp571Arg
ENST00000505084.2:n.1713T>C
ENST00000505350.2:c.*1663T>C	ENSP00000481752.1:n.*1663T>C
ENST00000507379.6:c.1603T>C	ENSP00000423224.2:p.Trp535Arg
ENST00000509732.6:c.1657T>C	ENSP00000426541.2:p.Trp553Arg
ENST00000512211.7:c.1657T>C	ENSP00000423828.3:p.Trp553Arg
ENST00000257430.9:c.1657T>C MANE Select	ENSP00000257430.4:p.Trp553Arg
ENST00000257430.8:c.1657T>C	ENSP00000257430.4:p.Trp553Arg
ENST00000502371.2:c.97-6065T>C
ENST00000504915.2:c.346T>C	ENSP00000473355.1:p.Trp116Arg
ENST00000505084.1:n.144T>C
ENST00000507379.5:c.1603T>C	ENSP00000423224.1:p.Trp535Arg
ENST00000508376.6:c.1657T>C	ENSP00000427089.2:p.Trp553Arg
ENST00000508624.5:c.*979T>C	ENSP00000424265.1:n.*979T>C
ENST00000512211.6:c.1657T>C	ENSP00000423828.2:p.Trp553Arg
ENST00000520401.1:c.144T>C
NM_000038.5:c.1657T>C	NP_000029.2:p.Trp553Arg
NM_001127510.2:c.1657T>C	NP_001120982.1:p.Trp553Arg
NM_001127511.2:c.1603T>C	NP_001120983.2:p.Trp535Arg
NM_001354895.1:c.1657T>C	NP_001341824.1:p.Trp553Arg
NM_001354896.1:c.1711T>C	NP_001341825.1:p.Trp571Arg
NM_001354897.1:c.1687T>C	NP_001341826.1:p.Trp563Arg
NM_001354898.1:c.1582T>C	NP_001341827.1:p.Trp528Arg
NM_001354899.1:c.1573T>C	NP_001341828.1:p.Trp525Arg
NM_001354900.1:c.1534T>C	NP_001341829.1:p.Trp512Arg
NM_001354901.1:c.1480T>C	NP_001341830.1:p.Trp494Arg
NM_001354902.1:c.1384T>C	NP_001341831.1:p.Trp462Arg
NM_001354903.1:c.1354T>C	NP_001341832.1:p.Trp452Arg
NM_001354904.1:c.1279T>C	NP_001341833.1:p.Trp427Arg
NM_001354905.1:c.1177T>C	NP_001341834.1:p.Trp393Arg
NM_001354906.1:c.808T>C	NP_001341835.1:p.Trp270Arg
NM_000038.6:c.1657T>C MANE Select	NP_000029.2:p.Trp553Arg
NM_001127510.3:c.1657T>C	NP_001120982.1:p.Trp553Arg
NM_001127511.3:c.1603T>C	NP_001120983.2:p.Trp535Arg
NM_001354895.2:c.1657T>C	NP_001341824.1:p.Trp553Arg
NM_001354896.2:c.1711T>C	NP_001341825.1:p.Trp571Arg
NM_001354897.2:c.1687T>C	NP_001341826.1:p.Trp563Arg
NM_001354898.2:c.1582T>C	NP_001341827.1:p.Trp528Arg
NM_001354899.2:c.1573T>C	NP_001341828.1:p.Trp525Arg
NM_001354900.2:c.1534T>C	NP_001341829.1:p.Trp512Arg
NM_001354901.2:c.1480T>C	NP_001341830.1:p.Trp494Arg
NM_001354902.2:c.1384T>C	NP_001341831.1:p.Trp462Arg
NM_001354903.2:c.1354T>C	NP_001341832.1:p.Trp452Arg
NM_001354904.2:c.1279T>C	NP_001341833.1:p.Trp427Arg
NM_001354905.2:c.1177T>C	NP_001341834.1:p.Trp393Arg
NM_001354906.2:c.808T>C	NP_001341835.1:p.Trp270Arg