Canonical Allele Identifier: CA16025239

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112170697A>C (hg19) ; chr5:g.112835000A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835000A>C , CM000667.2:g.112835000A>C	GRCh38
NC_000005.9:g.112170697A>C , CM000667.1:g.112170697A>C	GRCh37
NC_000005.8:g.112198596A>C	NCBI36
NG_008481.4:g.147480A>C , LRG_130:g.147480A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1458A>C	ENSP00000484935.2:p.Thr486=
ENST00000504915.3:c.1847A>C	ENSP00000473355.2:p.His616Pro
ENST00000505350.2:c.*1799A>C	ENSP00000481752.1:n.*1799A>C
ENST00000507379.6:c.1739A>C	ENSP00000423224.2:p.His580Pro
ENST00000509732.6:c.1793A>C	ENSP00000426541.2:p.His598Pro
ENST00000512211.7:c.1793A>C	ENSP00000423828.3:p.His598Pro
ENST00000257430.9:c.1793A>C MANE Select	ENSP00000257430.4:p.His598Pro
ENST00000257430.8:c.1793A>C	ENSP00000257430.4:p.His598Pro
ENST00000502371.2:c.146A>C
ENST00000504915.2:c.482A>C	ENSP00000473355.1:p.His161Pro
ENST00000507379.5:c.1739A>C	ENSP00000423224.1:p.His580Pro
ENST00000508376.6:c.1793A>C	ENSP00000427089.2:p.His598Pro
ENST00000508624.5:c.*1115A>C	ENSP00000424265.1:n.*1115A>C
ENST00000512211.6:c.1793A>C	ENSP00000423828.2:p.His598Pro
ENST00000520401.1:c.230+6028A>C
NM_000038.5:c.1793A>C	NP_000029.2:p.His598Pro
NM_001127510.2:c.1793A>C	NP_001120982.1:p.His598Pro
NM_001127511.2:c.1739A>C	NP_001120983.2:p.His580Pro
NM_001354895.1:c.1793A>C	NP_001341824.1:p.His598Pro
NM_001354896.1:c.1847A>C	NP_001341825.1:p.His616Pro
NM_001354897.1:c.1823A>C	NP_001341826.1:p.His608Pro
NM_001354898.1:c.1718A>C	NP_001341827.1:p.His573Pro
NM_001354899.1:c.1709A>C	NP_001341828.1:p.His570Pro
NM_001354900.1:c.1670A>C	NP_001341829.1:p.His557Pro
NM_001354901.1:c.1616A>C	NP_001341830.1:p.His539Pro
NM_001354902.1:c.1520A>C	NP_001341831.1:p.His507Pro
NM_001354903.1:c.1490A>C	NP_001341832.1:p.His497Pro
NM_001354904.1:c.1415A>C	NP_001341833.1:p.His472Pro
NM_001354905.1:c.1313A>C	NP_001341834.1:p.His438Pro
NM_001354906.1:c.944A>C	NP_001341835.1:p.His315Pro
NM_000038.6:c.1793A>C MANE Select	NP_000029.2:p.His598Pro
NM_001127510.3:c.1793A>C	NP_001120982.1:p.His598Pro
NM_001127511.3:c.1739A>C	NP_001120983.2:p.His580Pro
NM_001354895.2:c.1793A>C	NP_001341824.1:p.His598Pro
NM_001354896.2:c.1847A>C	NP_001341825.1:p.His616Pro
NM_001354897.2:c.1823A>C	NP_001341826.1:p.His608Pro
NM_001354898.2:c.1718A>C	NP_001341827.1:p.His573Pro
NM_001354899.2:c.1709A>C	NP_001341828.1:p.His570Pro
NM_001354900.2:c.1670A>C	NP_001341829.1:p.His557Pro
NM_001354901.2:c.1616A>C	NP_001341830.1:p.His539Pro
NM_001354902.2:c.1520A>C	NP_001341831.1:p.His507Pro
NM_001354903.2:c.1490A>C	NP_001341832.1:p.His497Pro
NM_001354904.2:c.1415A>C	NP_001341833.1:p.His472Pro
NM_001354905.2:c.1313A>C	NP_001341834.1:p.His438Pro
NM_001354906.2:c.944A>C	NP_001341835.1:p.His315Pro