Canonical Allele Identifier: CA16032447

Gene: APC

Linked Data

• dbSNP Id: rs1554086438
• MyVariant Identifiers: chr5:g.112176376A>C (hg19) ; chr5:g.112840679A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840679A>C , CM000667.2:g.112840679A>C	GRCh38
NC_000005.9:g.112176376A>C , CM000667.1:g.112176376A>C	GRCh37
NC_000005.8:g.112204275A>C	NCBI36
NG_008481.4:g.153159A>C , LRG_130:g.153159A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5139A>C	ENSP00000473355.2:p.Arg1713Ser
ENST00000505350.2:c.*5091A>C	ENSP00000481752.1:n.*5091A>C
ENST00000507379.6:c.5031A>C	ENSP00000423224.2:p.Arg1677Ser
ENST00000509732.6:c.5085A>C	ENSP00000426541.2:p.Arg1695Ser
ENST00000512211.7:c.5085A>C	ENSP00000423828.3:p.Arg1695Ser
ENST00000257430.9:c.5085A>C MANE Select	ENSP00000257430.4:p.Arg1695Ser
ENST00000257430.8:c.5085A>C	ENSP00000257430.4:p.Arg1695Ser
ENST00000508376.6:c.5085A>C	ENSP00000427089.2:p.Arg1695Ser
ENST00000508624.5:c.*4407A>C	ENSP00000424265.1:n.*4407A>C
ENST00000520401.1:c.230+11707A>C
NM_000038.5:c.5085A>C	NP_000029.2:p.Arg1695Ser
NM_001127510.2:c.5085A>C	NP_001120982.1:p.Arg1695Ser
NM_001127511.2:c.5031A>C	NP_001120983.2:p.Arg1677Ser
NM_001354895.1:c.5085A>C	NP_001341824.1:p.Arg1695Ser
NM_001354896.1:c.5139A>C	NP_001341825.1:p.Arg1713Ser
NM_001354897.1:c.5115A>C	NP_001341826.1:p.Arg1705Ser
NM_001354898.1:c.5010A>C	NP_001341827.1:p.Arg1670Ser
NM_001354899.1:c.5001A>C	NP_001341828.1:p.Arg1667Ser
NM_001354900.1:c.4962A>C	NP_001341829.1:p.Arg1654Ser
NM_001354901.1:c.4908A>C	NP_001341830.1:p.Arg1636Ser
NM_001354902.1:c.4812A>C	NP_001341831.1:p.Arg1604Ser
NM_001354903.1:c.4782A>C	NP_001341832.1:p.Arg1594Ser
NM_001354904.1:c.4707A>C	NP_001341833.1:p.Arg1569Ser
NM_001354905.1:c.4605A>C	NP_001341834.1:p.Arg1535Ser
NM_001354906.1:c.4236A>C	NP_001341835.1:p.Arg1412Ser
NM_000038.6:c.5085A>C MANE Select	NP_000029.2:p.Arg1695Ser
NM_001127510.3:c.5085A>C	NP_001120982.1:p.Arg1695Ser
NM_001127511.3:c.5031A>C	NP_001120983.2:p.Arg1677Ser
NM_001354895.2:c.5085A>C	NP_001341824.1:p.Arg1695Ser
NM_001354896.2:c.5139A>C	NP_001341825.1:p.Arg1713Ser
NM_001354897.2:c.5115A>C	NP_001341826.1:p.Arg1705Ser
NM_001354898.2:c.5010A>C	NP_001341827.1:p.Arg1670Ser
NM_001354899.2:c.5001A>C	NP_001341828.1:p.Arg1667Ser
NM_001354900.2:c.4962A>C	NP_001341829.1:p.Arg1654Ser
NM_001354901.2:c.4908A>C	NP_001341830.1:p.Arg1636Ser
NM_001354902.2:c.4812A>C	NP_001341831.1:p.Arg1604Ser
NM_001354903.2:c.4782A>C	NP_001341832.1:p.Arg1594Ser
NM_001354904.2:c.4707A>C	NP_001341833.1:p.Arg1569Ser
NM_001354905.2:c.4605A>C	NP_001341834.1:p.Arg1535Ser
NM_001354906.2:c.4236A>C	NP_001341835.1:p.Arg1412Ser