Canonical Allele Identifier: CA16031894

Gene: APC

Linked Data

• dbSNP Id: rs2149924660
• COSMIC: COSM6475521
• MyVariant Identifiers: chr5:g.112176112G>T (hg19) ; chr5:g.112840415G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840415G>T , CM000667.2:g.112840415G>T	GRCh38
NC_000005.9:g.112176112G>T , CM000667.1:g.112176112G>T	GRCh37
NC_000005.8:g.112204011G>T	NCBI36
NG_008481.4:g.152895G>T , LRG_130:g.152895G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.4875G>T	ENSP00000473355.2:p.Arg1625Ser
ENST00000505350.2:c.*4827G>T	ENSP00000481752.1:n.*4827G>T
ENST00000507379.6:c.4767G>T	ENSP00000423224.2:p.Arg1589Ser
ENST00000509732.6:c.4821G>T	ENSP00000426541.2:p.Arg1607Ser
ENST00000512211.7:c.4821G>T	ENSP00000423828.3:p.Arg1607Ser
ENST00000257430.9:c.4821G>T MANE Select	ENSP00000257430.4:p.Arg1607Ser
ENST00000257430.8:c.4821G>T	ENSP00000257430.4:p.Arg1607Ser
ENST00000508376.6:c.4821G>T	ENSP00000427089.2:p.Arg1607Ser
ENST00000508624.5:c.*4143G>T	ENSP00000424265.1:n.*4143G>T
ENST00000520401.1:c.230+11443G>T
NM_000038.5:c.4821G>T	NP_000029.2:p.Arg1607Ser
NM_001127510.2:c.4821G>T	NP_001120982.1:p.Arg1607Ser
NM_001127511.2:c.4767G>T	NP_001120983.2:p.Arg1589Ser
NM_001354895.1:c.4821G>T	NP_001341824.1:p.Arg1607Ser
NM_001354896.1:c.4875G>T	NP_001341825.1:p.Arg1625Ser
NM_001354897.1:c.4851G>T	NP_001341826.1:p.Arg1617Ser
NM_001354898.1:c.4746G>T	NP_001341827.1:p.Arg1582Ser
NM_001354899.1:c.4737G>T	NP_001341828.1:p.Arg1579Ser
NM_001354900.1:c.4698G>T	NP_001341829.1:p.Arg1566Ser
NM_001354901.1:c.4644G>T	NP_001341830.1:p.Arg1548Ser
NM_001354902.1:c.4548G>T	NP_001341831.1:p.Arg1516Ser
NM_001354903.1:c.4518G>T	NP_001341832.1:p.Arg1506Ser
NM_001354904.1:c.4443G>T	NP_001341833.1:p.Arg1481Ser
NM_001354905.1:c.4341G>T	NP_001341834.1:p.Arg1447Ser
NM_001354906.1:c.3972G>T	NP_001341835.1:p.Arg1324Ser
NM_000038.6:c.4821G>T MANE Select	NP_000029.2:p.Arg1607Ser
NM_001127510.3:c.4821G>T	NP_001120982.1:p.Arg1607Ser
NM_001127511.3:c.4767G>T	NP_001120983.2:p.Arg1589Ser
NM_001354895.2:c.4821G>T	NP_001341824.1:p.Arg1607Ser
NM_001354896.2:c.4875G>T	NP_001341825.1:p.Arg1625Ser
NM_001354897.2:c.4851G>T	NP_001341826.1:p.Arg1617Ser
NM_001354898.2:c.4746G>T	NP_001341827.1:p.Arg1582Ser
NM_001354899.2:c.4737G>T	NP_001341828.1:p.Arg1579Ser
NM_001354900.2:c.4698G>T	NP_001341829.1:p.Arg1566Ser
NM_001354901.2:c.4644G>T	NP_001341830.1:p.Arg1548Ser
NM_001354902.2:c.4548G>T	NP_001341831.1:p.Arg1516Ser
NM_001354903.2:c.4518G>T	NP_001341832.1:p.Arg1506Ser
NM_001354904.2:c.4443G>T	NP_001341833.1:p.Arg1481Ser
NM_001354905.2:c.4341G>T	NP_001341834.1:p.Arg1447Ser
NM_001354906.2:c.3972G>T	NP_001341835.1:p.Arg1324Ser