Canonical Allele Identifier: CA16039016

Gene: APC

Linked Data

• dbSNP Id: rs587780605
• MyVariant Identifiers: chr5:g.112179435C>A (hg19) ; chr5:g.112843738C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843738C>A , CM000667.2:g.112843738C>A	GRCh38
NC_000005.9:g.112179435C>A , CM000667.1:g.112179435C>A	GRCh37
NC_000005.8:g.112207334C>A	NCBI36
NG_008481.4:g.156218C>A , LRG_130:g.156218C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8198C>A	ENSP00000473355.2:p.Thr2733Asn
ENST00000505350.2:c.*8150C>A	ENSP00000481752.1:n.*8150C>A
ENST00000507379.6:c.8090C>A	ENSP00000423224.2:p.Thr2697Asn
ENST00000509732.6:c.8144C>A	ENSP00000426541.2:p.Thr2715Asn
ENST00000512211.7:c.8144C>A	ENSP00000423828.3:p.Thr2715Asn
ENST00000257430.9:c.8144C>A MANE Select	ENSP00000257430.4:p.Thr2715Asn
ENST00000257430.8:c.8144C>A	ENSP00000257430.4:p.Thr2715Asn
ENST00000508376.6:c.8144C>A	ENSP00000427089.2:p.Thr2715Asn
ENST00000520401.1:c.231-12911C>A
NM_000038.5:c.8144C>A	NP_000029.2:p.Thr2715Asn
NM_001127510.2:c.8144C>A	NP_001120982.1:p.Thr2715Asn
NM_001127511.2:c.8090C>A	NP_001120983.2:p.Thr2697Asn
NM_001354895.1:c.8144C>A	NP_001341824.1:p.Thr2715Asn
NM_001354896.1:c.8198C>A	NP_001341825.1:p.Thr2733Asn
NM_001354897.1:c.8174C>A	NP_001341826.1:p.Thr2725Asn
NM_001354898.1:c.8069C>A	NP_001341827.1:p.Thr2690Asn
NM_001354899.1:c.8060C>A	NP_001341828.1:p.Thr2687Asn
NM_001354900.1:c.8021C>A	NP_001341829.1:p.Thr2674Asn
NM_001354901.1:c.7967C>A	NP_001341830.1:p.Thr2656Asn
NM_001354902.1:c.7871C>A	NP_001341831.1:p.Thr2624Asn
NM_001354903.1:c.7841C>A	NP_001341832.1:p.Thr2614Asn
NM_001354904.1:c.7766C>A	NP_001341833.1:p.Thr2589Asn
NM_001354905.1:c.7664C>A	NP_001341834.1:p.Thr2555Asn
NM_001354906.1:c.7295C>A	NP_001341835.1:p.Thr2432Asn
NM_000038.6:c.8144C>A MANE Select	NP_000029.2:p.Thr2715Asn
NM_001127510.3:c.8144C>A	NP_001120982.1:p.Thr2715Asn
NM_001127511.3:c.8090C>A	NP_001120983.2:p.Thr2697Asn
NM_001354895.2:c.8144C>A	NP_001341824.1:p.Thr2715Asn
NM_001354896.2:c.8198C>A	NP_001341825.1:p.Thr2733Asn
NM_001354897.2:c.8174C>A	NP_001341826.1:p.Thr2725Asn
NM_001354898.2:c.8069C>A	NP_001341827.1:p.Thr2690Asn
NM_001354899.2:c.8060C>A	NP_001341828.1:p.Thr2687Asn
NM_001354900.2:c.8021C>A	NP_001341829.1:p.Thr2674Asn
NM_001354901.2:c.7967C>A	NP_001341830.1:p.Thr2656Asn
NM_001354902.2:c.7871C>A	NP_001341831.1:p.Thr2624Asn
NM_001354903.2:c.7841C>A	NP_001341832.1:p.Thr2614Asn
NM_001354904.2:c.7766C>A	NP_001341833.1:p.Thr2589Asn
NM_001354905.2:c.7664C>A	NP_001341834.1:p.Thr2555Asn
NM_001354906.2:c.7295C>A	NP_001341835.1:p.Thr2432Asn