Canonical Allele Identifier: CA16031552

Gene: APC

Linked Data

• dbSNP Id: rs2149920450
• MyVariant Identifiers: chr5:g.112175953A>T (hg19) ; chr5:g.112840256A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840256A>T , CM000667.2:g.112840256A>T	GRCh38
NC_000005.9:g.112175953A>T , CM000667.1:g.112175953A>T	GRCh37
NC_000005.8:g.112203852A>T	NCBI36
NG_008481.4:g.152736A>T , LRG_130:g.152736A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4716A>T	ENSP00000473355.2:p.Glu1572Asp
ENST00000505350.2:c.*4668A>T	ENSP00000481752.1:n.*4668A>T
ENST00000507379.6:c.4608A>T	ENSP00000423224.2:p.Glu1536Asp
ENST00000509732.6:c.4662A>T	ENSP00000426541.2:p.Glu1554Asp
ENST00000512211.7:c.4662A>T	ENSP00000423828.3:p.Glu1554Asp
ENST00000257430.9:c.4662A>T MANE Select	ENSP00000257430.4:p.Glu1554Asp
ENST00000257430.8:c.4662A>T	ENSP00000257430.4:p.Glu1554Asp
ENST00000508376.6:c.4662A>T	ENSP00000427089.2:p.Glu1554Asp
ENST00000508624.5:c.*3984A>T	ENSP00000424265.1:n.*3984A>T
ENST00000520401.1:c.230+11284A>T
NM_000038.5:c.4662A>T	NP_000029.2:p.Glu1554Asp
NM_001127510.2:c.4662A>T	NP_001120982.1:p.Glu1554Asp
NM_001127511.2:c.4608A>T	NP_001120983.2:p.Glu1536Asp
NM_001354895.1:c.4662A>T	NP_001341824.1:p.Glu1554Asp
NM_001354896.1:c.4716A>T	NP_001341825.1:p.Glu1572Asp
NM_001354897.1:c.4692A>T	NP_001341826.1:p.Glu1564Asp
NM_001354898.1:c.4587A>T	NP_001341827.1:p.Glu1529Asp
NM_001354899.1:c.4578A>T	NP_001341828.1:p.Glu1526Asp
NM_001354900.1:c.4539A>T	NP_001341829.1:p.Glu1513Asp
NM_001354901.1:c.4485A>T	NP_001341830.1:p.Glu1495Asp
NM_001354902.1:c.4389A>T	NP_001341831.1:p.Glu1463Asp
NM_001354903.1:c.4359A>T	NP_001341832.1:p.Glu1453Asp
NM_001354904.1:c.4284A>T	NP_001341833.1:p.Glu1428Asp
NM_001354905.1:c.4182A>T	NP_001341834.1:p.Glu1394Asp
NM_001354906.1:c.3813A>T	NP_001341835.1:p.Glu1271Asp
NM_000038.6:c.4662A>T MANE Select	NP_000029.2:p.Glu1554Asp
NM_001127510.3:c.4662A>T	NP_001120982.1:p.Glu1554Asp
NM_001127511.3:c.4608A>T	NP_001120983.2:p.Glu1536Asp
NM_001354895.2:c.4662A>T	NP_001341824.1:p.Glu1554Asp
NM_001354896.2:c.4716A>T	NP_001341825.1:p.Glu1572Asp
NM_001354897.2:c.4692A>T	NP_001341826.1:p.Glu1564Asp
NM_001354898.2:c.4587A>T	NP_001341827.1:p.Glu1529Asp
NM_001354899.2:c.4578A>T	NP_001341828.1:p.Glu1526Asp
NM_001354900.2:c.4539A>T	NP_001341829.1:p.Glu1513Asp
NM_001354901.2:c.4485A>T	NP_001341830.1:p.Glu1495Asp
NM_001354902.2:c.4389A>T	NP_001341831.1:p.Glu1463Asp
NM_001354903.2:c.4359A>T	NP_001341832.1:p.Glu1453Asp
NM_001354904.2:c.4284A>T	NP_001341833.1:p.Glu1428Asp
NM_001354905.2:c.4182A>T	NP_001341834.1:p.Glu1394Asp
NM_001354906.2:c.3813A>T	NP_001341835.1:p.Glu1271Asp