Canonical Allele Identifier: CA16029955

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112175220A>C (hg19) ; chr5:g.112839523A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839523A>C , CM000667.2:g.112839523A>C	GRCh38
NC_000005.9:g.112175220A>C , CM000667.1:g.112175220A>C	GRCh37
NC_000005.8:g.112203119A>C	NCBI36
NG_008481.4:g.152003A>C , LRG_130:g.152003A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3594A>C	ENSP00000484935.2:n.3594A>C
ENST00000504915.3:c.3983A>C	ENSP00000473355.2:p.Lys1328Thr
ENST00000505350.2:c.*3935A>C	ENSP00000481752.1:n.*3935A>C
ENST00000507379.6:c.3875A>C	ENSP00000423224.2:p.Lys1292Thr
ENST00000509732.6:c.3929A>C	ENSP00000426541.2:p.Lys1310Thr
ENST00000512211.7:c.3929A>C	ENSP00000423828.3:p.Lys1310Thr
ENST00000257430.9:c.3929A>C MANE Select	ENSP00000257430.4:p.Lys1310Thr
ENST00000257430.8:c.3929A>C	ENSP00000257430.4:p.Lys1310Thr
ENST00000502371.2:c.2282A>C
ENST00000508376.6:c.3929A>C	ENSP00000427089.2:p.Lys1310Thr
ENST00000508624.5:c.*3251A>C	ENSP00000424265.1:n.*3251A>C
ENST00000520401.1:c.230+10551A>C
NM_000038.5:c.3929A>C	NP_000029.2:p.Lys1310Thr
NM_001127510.2:c.3929A>C	NP_001120982.1:p.Lys1310Thr
NM_001127511.2:c.3875A>C	NP_001120983.2:p.Lys1292Thr
NM_001354895.1:c.3929A>C	NP_001341824.1:p.Lys1310Thr
NM_001354896.1:c.3983A>C	NP_001341825.1:p.Lys1328Thr
NM_001354897.1:c.3959A>C	NP_001341826.1:p.Lys1320Thr
NM_001354898.1:c.3854A>C	NP_001341827.1:p.Lys1285Thr
NM_001354899.1:c.3845A>C	NP_001341828.1:p.Lys1282Thr
NM_001354900.1:c.3806A>C	NP_001341829.1:p.Lys1269Thr
NM_001354901.1:c.3752A>C	NP_001341830.1:p.Lys1251Thr
NM_001354902.1:c.3656A>C	NP_001341831.1:p.Lys1219Thr
NM_001354903.1:c.3626A>C	NP_001341832.1:p.Lys1209Thr
NM_001354904.1:c.3551A>C	NP_001341833.1:p.Lys1184Thr
NM_001354905.1:c.3449A>C	NP_001341834.1:p.Lys1150Thr
NM_001354906.1:c.3080A>C	NP_001341835.1:p.Lys1027Thr
NM_000038.6:c.3929A>C MANE Select	NP_000029.2:p.Lys1310Thr
NM_001127510.3:c.3929A>C	NP_001120982.1:p.Lys1310Thr
NM_001127511.3:c.3875A>C	NP_001120983.2:p.Lys1292Thr
NM_001354895.2:c.3929A>C	NP_001341824.1:p.Lys1310Thr
NM_001354896.2:c.3983A>C	NP_001341825.1:p.Lys1328Thr
NM_001354897.2:c.3959A>C	NP_001341826.1:p.Lys1320Thr
NM_001354898.2:c.3854A>C	NP_001341827.1:p.Lys1285Thr
NM_001354899.2:c.3845A>C	NP_001341828.1:p.Lys1282Thr
NM_001354900.2:c.3806A>C	NP_001341829.1:p.Lys1269Thr
NM_001354901.2:c.3752A>C	NP_001341830.1:p.Lys1251Thr
NM_001354902.2:c.3656A>C	NP_001341831.1:p.Lys1219Thr
NM_001354903.2:c.3626A>C	NP_001341832.1:p.Lys1209Thr
NM_001354904.2:c.3551A>C	NP_001341833.1:p.Lys1184Thr
NM_001354905.2:c.3449A>C	NP_001341834.1:p.Lys1150Thr
NM_001354906.2:c.3080A>C	NP_001341835.1:p.Lys1027Thr