Canonical Allele Identifier: CA16036708

Gene: APC

Linked Data

• dbSNP Id: rs2149979100
• MyVariant Identifiers: chr5:g.112178348A>C (hg19) ; chr5:g.112842651A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112842651A>C , CM000667.2:g.112842651A>C	GRCh38
NC_000005.9:g.112178348A>C , CM000667.1:g.112178348A>C	GRCh37
NC_000005.8:g.112206247A>C	NCBI36
NG_008481.4:g.155131A>C , LRG_130:g.155131A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7111A>C	ENSP00000473355.2:p.Thr2371Pro
ENST00000505350.2:c.*7063A>C	ENSP00000481752.1:n.*7063A>C
ENST00000507379.6:c.7003A>C	ENSP00000423224.2:p.Thr2335Pro
ENST00000509732.6:c.7057A>C	ENSP00000426541.2:p.Thr2353Pro
ENST00000512211.7:c.7057A>C	ENSP00000423828.3:p.Thr2353Pro
ENST00000257430.9:c.7057A>C MANE Select	ENSP00000257430.4:p.Thr2353Pro
ENST00000257430.8:c.7057A>C	ENSP00000257430.4:p.Thr2353Pro
ENST00000508376.6:c.7057A>C	ENSP00000427089.2:p.Thr2353Pro
ENST00000508624.5:c.*6379A>C	ENSP00000424265.1:n.*6379A>C
ENST00000520401.1:c.230+13679A>C
NM_000038.5:c.7057A>C	NP_000029.2:p.Thr2353Pro
NM_001127510.2:c.7057A>C	NP_001120982.1:p.Thr2353Pro
NM_001127511.2:c.7003A>C	NP_001120983.2:p.Thr2335Pro
NM_001354895.1:c.7057A>C	NP_001341824.1:p.Thr2353Pro
NM_001354896.1:c.7111A>C	NP_001341825.1:p.Thr2371Pro
NM_001354897.1:c.7087A>C	NP_001341826.1:p.Thr2363Pro
NM_001354898.1:c.6982A>C	NP_001341827.1:p.Thr2328Pro
NM_001354899.1:c.6973A>C	NP_001341828.1:p.Thr2325Pro
NM_001354900.1:c.6934A>C	NP_001341829.1:p.Thr2312Pro
NM_001354901.1:c.6880A>C	NP_001341830.1:p.Thr2294Pro
NM_001354902.1:c.6784A>C	NP_001341831.1:p.Thr2262Pro
NM_001354903.1:c.6754A>C	NP_001341832.1:p.Thr2252Pro
NM_001354904.1:c.6679A>C	NP_001341833.1:p.Thr2227Pro
NM_001354905.1:c.6577A>C	NP_001341834.1:p.Thr2193Pro
NM_001354906.1:c.6208A>C	NP_001341835.1:p.Thr2070Pro
NM_000038.6:c.7057A>C MANE Select	NP_000029.2:p.Thr2353Pro
NM_001127510.3:c.7057A>C	NP_001120982.1:p.Thr2353Pro
NM_001127511.3:c.7003A>C	NP_001120983.2:p.Thr2335Pro
NM_001354895.2:c.7057A>C	NP_001341824.1:p.Thr2353Pro
NM_001354896.2:c.7111A>C	NP_001341825.1:p.Thr2371Pro
NM_001354897.2:c.7087A>C	NP_001341826.1:p.Thr2363Pro
NM_001354898.2:c.6982A>C	NP_001341827.1:p.Thr2328Pro
NM_001354899.2:c.6973A>C	NP_001341828.1:p.Thr2325Pro
NM_001354900.2:c.6934A>C	NP_001341829.1:p.Thr2312Pro
NM_001354901.2:c.6880A>C	NP_001341830.1:p.Thr2294Pro
NM_001354902.2:c.6784A>C	NP_001341831.1:p.Thr2262Pro
NM_001354903.2:c.6754A>C	NP_001341832.1:p.Thr2252Pro
NM_001354904.2:c.6679A>C	NP_001341833.1:p.Thr2227Pro
NM_001354905.2:c.6577A>C	NP_001341834.1:p.Thr2193Pro
NM_001354906.2:c.6208A>C	NP_001341835.1:p.Thr2070Pro