Canonical Allele Identifier: CA446210987

Gene: APC

Linked Data

• dbSNP Id: rs2149997034
• MyVariant Identifiers: chr5:g.112179253A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843556A>T , CM000667.2:g.112843556A>T	GRCh38
NC_000005.9:g.112179253A>T , CM000667.1:g.112179253A>T	GRCh37
NC_000005.8:g.112207152A>T	NCBI36
NG_008481.4:g.156036A>T , LRG_130:g.156036A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8016A>T	ENSP00000473355.2:p.Thr2672=
ENST00000505350.2:c.*7968A>T	ENSP00000481752.1:n.*7968A>T
ENST00000507379.6:c.7908A>T	ENSP00000423224.2:p.Thr2636=
ENST00000509732.6:c.7962A>T	ENSP00000426541.2:p.Thr2654=
ENST00000512211.7:c.7962A>T	ENSP00000423828.3:p.Thr2654=
ENST00000257430.9:c.7962A>T MANE Select	ENSP00000257430.4:p.Thr2654=
ENST00000257430.8:c.7962A>T	ENSP00000257430.4:p.Thr2654=
ENST00000508376.6:c.7962A>T	ENSP00000427089.2:p.Thr2654=
ENST00000520401.1:c.231-13093A>T
NM_000038.5:c.7962A>T	NP_000029.2:p.Thr2654=
NM_001127510.2:c.7962A>T	NP_001120982.1:p.Thr2654=
NM_001127511.2:c.7908A>T	NP_001120983.2:p.Thr2636=
NM_001354895.1:c.7962A>T	NP_001341824.1:p.Thr2654=
NM_001354896.1:c.8016A>T	NP_001341825.1:p.Thr2672=
NM_001354897.1:c.7992A>T	NP_001341826.1:p.Thr2664=
NM_001354898.1:c.7887A>T	NP_001341827.1:p.Thr2629=
NM_001354899.1:c.7878A>T	NP_001341828.1:p.Thr2626=
NM_001354900.1:c.7839A>T	NP_001341829.1:p.Thr2613=
NM_001354901.1:c.7785A>T	NP_001341830.1:p.Thr2595=
NM_001354902.1:c.7689A>T	NP_001341831.1:p.Thr2563=
NM_001354903.1:c.7659A>T	NP_001341832.1:p.Thr2553=
NM_001354904.1:c.7584A>T	NP_001341833.1:p.Thr2528=
NM_001354905.1:c.7482A>T	NP_001341834.1:p.Thr2494=
NM_001354906.1:c.7113A>T	NP_001341835.1:p.Thr2371=
NM_000038.6:c.7962A>T MANE Select	NP_000029.2:p.Thr2654=
NM_001127510.3:c.7962A>T	NP_001120982.1:p.Thr2654=
NM_001127511.3:c.7908A>T	NP_001120983.2:p.Thr2636=
NM_001354895.2:c.7962A>T	NP_001341824.1:p.Thr2654=
NM_001354896.2:c.8016A>T	NP_001341825.1:p.Thr2672=
NM_001354897.2:c.7992A>T	NP_001341826.1:p.Thr2664=
NM_001354898.2:c.7887A>T	NP_001341827.1:p.Thr2629=
NM_001354899.2:c.7878A>T	NP_001341828.1:p.Thr2626=
NM_001354900.2:c.7839A>T	NP_001341829.1:p.Thr2613=
NM_001354901.2:c.7785A>T	NP_001341830.1:p.Thr2595=
NM_001354902.2:c.7689A>T	NP_001341831.1:p.Thr2563=
NM_001354903.2:c.7659A>T	NP_001341832.1:p.Thr2553=
NM_001354904.2:c.7584A>T	NP_001341833.1:p.Thr2528=
NM_001354905.2:c.7482A>T	NP_001341834.1:p.Thr2494=
NM_001354906.2:c.7113A>T	NP_001341835.1:p.Thr2371=