Canonical Allele Identifier: CA16025280

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112170713A>C (hg19) ; chr5:g.112835016A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835016A>C , CM000667.2:g.112835016A>C	GRCh38
NC_000005.9:g.112170713A>C , CM000667.1:g.112170713A>C	GRCh37
NC_000005.8:g.112198612A>C	NCBI36
NG_008481.4:g.147496A>C , LRG_130:g.147496A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1474A>C	ENSP00000484935.2:n.1474A>C
ENST00000504915.3:c.1863A>C	ENSP00000473355.2:p.Lys621Asn
ENST00000505350.2:c.*1815A>C	ENSP00000481752.1:n.*1815A>C
ENST00000507379.6:c.1755A>C	ENSP00000423224.2:p.Lys585Asn
ENST00000509732.6:c.1809A>C	ENSP00000426541.2:p.Lys603Asn
ENST00000512211.7:c.1809A>C	ENSP00000423828.3:p.Lys603Asn
ENST00000257430.9:c.1809A>C MANE Select	ENSP00000257430.4:p.Lys603Asn
ENST00000257430.8:c.1809A>C	ENSP00000257430.4:p.Lys603Asn
ENST00000502371.2:c.162A>C
ENST00000504915.2:c.498A>C	ENSP00000473355.1:p.Lys166Asn
ENST00000507379.5:c.1755A>C	ENSP00000423224.1:p.Lys585Asn
ENST00000508376.6:c.1809A>C	ENSP00000427089.2:p.Lys603Asn
ENST00000508624.5:c.*1131A>C	ENSP00000424265.1:n.*1131A>C
ENST00000512211.6:c.1809A>C	ENSP00000423828.2:p.Lys603Asn
ENST00000520401.1:c.230+6044A>C
NM_000038.5:c.1809A>C	NP_000029.2:p.Lys603Asn
NM_001127510.2:c.1809A>C	NP_001120982.1:p.Lys603Asn
NM_001127511.2:c.1755A>C	NP_001120983.2:p.Lys585Asn
NM_001354895.1:c.1809A>C	NP_001341824.1:p.Lys603Asn
NM_001354896.1:c.1863A>C	NP_001341825.1:p.Lys621Asn
NM_001354897.1:c.1839A>C	NP_001341826.1:p.Lys613Asn
NM_001354898.1:c.1734A>C	NP_001341827.1:p.Lys578Asn
NM_001354899.1:c.1725A>C	NP_001341828.1:p.Lys575Asn
NM_001354900.1:c.1686A>C	NP_001341829.1:p.Lys562Asn
NM_001354901.1:c.1632A>C	NP_001341830.1:p.Lys544Asn
NM_001354902.1:c.1536A>C	NP_001341831.1:p.Lys512Asn
NM_001354903.1:c.1506A>C	NP_001341832.1:p.Lys502Asn
NM_001354904.1:c.1431A>C	NP_001341833.1:p.Lys477Asn
NM_001354905.1:c.1329A>C	NP_001341834.1:p.Lys443Asn
NM_001354906.1:c.960A>C	NP_001341835.1:p.Lys320Asn
NM_000038.6:c.1809A>C MANE Select	NP_000029.2:p.Lys603Asn
NM_001127510.3:c.1809A>C	NP_001120982.1:p.Lys603Asn
NM_001127511.3:c.1755A>C	NP_001120983.2:p.Lys585Asn
NM_001354895.2:c.1809A>C	NP_001341824.1:p.Lys603Asn
NM_001354896.2:c.1863A>C	NP_001341825.1:p.Lys621Asn
NM_001354897.2:c.1839A>C	NP_001341826.1:p.Lys613Asn
NM_001354898.2:c.1734A>C	NP_001341827.1:p.Lys578Asn
NM_001354899.2:c.1725A>C	NP_001341828.1:p.Lys575Asn
NM_001354900.2:c.1686A>C	NP_001341829.1:p.Lys562Asn
NM_001354901.2:c.1632A>C	NP_001341830.1:p.Lys544Asn
NM_001354902.2:c.1536A>C	NP_001341831.1:p.Lys512Asn
NM_001354903.2:c.1506A>C	NP_001341832.1:p.Lys502Asn
NM_001354904.2:c.1431A>C	NP_001341833.1:p.Lys477Asn
NM_001354905.2:c.1329A>C	NP_001341834.1:p.Lys443Asn
NM_001354906.2:c.960A>C	NP_001341835.1:p.Lys320Asn