Canonical Allele Identifier: CA16031576

Gene: APC

Linked Data

• dbSNP Id: rs2149920833
• MyVariant Identifiers: chr5:g.112175964A>T (hg19) ; chr5:g.112840267A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840267A>T , CM000667.2:g.112840267A>T	GRCh38
NC_000005.9:g.112175964A>T , CM000667.1:g.112175964A>T	GRCh37
NC_000005.8:g.112203863A>T	NCBI36
NG_008481.4:g.152747A>T , LRG_130:g.152747A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.4727A>T	ENSP00000473355.2:p.Asp1576Val
ENST00000505350.2:c.*4679A>T	ENSP00000481752.1:n.*4679A>T
ENST00000507379.6:c.4619A>T	ENSP00000423224.2:p.Asp1540Val
ENST00000509732.6:c.4673A>T	ENSP00000426541.2:p.Asp1558Val
ENST00000512211.7:c.4673A>T	ENSP00000423828.3:p.Asp1558Val
ENST00000257430.9:c.4673A>T MANE Select	ENSP00000257430.4:p.Asp1558Val
ENST00000257430.8:c.4673A>T	ENSP00000257430.4:p.Asp1558Val
ENST00000508376.6:c.4673A>T	ENSP00000427089.2:p.Asp1558Val
ENST00000508624.5:c.*3995A>T	ENSP00000424265.1:n.*3995A>T
ENST00000520401.1:c.230+11295A>T
NM_000038.5:c.4673A>T	NP_000029.2:p.Asp1558Val
NM_001127510.2:c.4673A>T	NP_001120982.1:p.Asp1558Val
NM_001127511.2:c.4619A>T	NP_001120983.2:p.Asp1540Val
NM_001354895.1:c.4673A>T	NP_001341824.1:p.Asp1558Val
NM_001354896.1:c.4727A>T	NP_001341825.1:p.Asp1576Val
NM_001354897.1:c.4703A>T	NP_001341826.1:p.Asp1568Val
NM_001354898.1:c.4598A>T	NP_001341827.1:p.Asp1533Val
NM_001354899.1:c.4589A>T	NP_001341828.1:p.Asp1530Val
NM_001354900.1:c.4550A>T	NP_001341829.1:p.Asp1517Val
NM_001354901.1:c.4496A>T	NP_001341830.1:p.Asp1499Val
NM_001354902.1:c.4400A>T	NP_001341831.1:p.Asp1467Val
NM_001354903.1:c.4370A>T	NP_001341832.1:p.Asp1457Val
NM_001354904.1:c.4295A>T	NP_001341833.1:p.Asp1432Val
NM_001354905.1:c.4193A>T	NP_001341834.1:p.Asp1398Val
NM_001354906.1:c.3824A>T	NP_001341835.1:p.Asp1275Val
NM_000038.6:c.4673A>T MANE Select	NP_000029.2:p.Asp1558Val
NM_001127510.3:c.4673A>T	NP_001120982.1:p.Asp1558Val
NM_001127511.3:c.4619A>T	NP_001120983.2:p.Asp1540Val
NM_001354895.2:c.4673A>T	NP_001341824.1:p.Asp1558Val
NM_001354896.2:c.4727A>T	NP_001341825.1:p.Asp1576Val
NM_001354897.2:c.4703A>T	NP_001341826.1:p.Asp1568Val
NM_001354898.2:c.4598A>T	NP_001341827.1:p.Asp1533Val
NM_001354899.2:c.4589A>T	NP_001341828.1:p.Asp1530Val
NM_001354900.2:c.4550A>T	NP_001341829.1:p.Asp1517Val
NM_001354901.2:c.4496A>T	NP_001341830.1:p.Asp1499Val
NM_001354902.2:c.4400A>T	NP_001341831.1:p.Asp1467Val
NM_001354903.2:c.4370A>T	NP_001341832.1:p.Asp1457Val
NM_001354904.2:c.4295A>T	NP_001341833.1:p.Asp1432Val
NM_001354905.2:c.4193A>T	NP_001341834.1:p.Asp1398Val
NM_001354906.2:c.3824A>T	NP_001341835.1:p.Asp1275Val