Canonical Allele Identifier: CA16036739

Gene: APC

Linked Data

• dbSNP Id: rs2149979397
• MyVariant Identifiers: chr5:g.112178363T>A (hg19) ; chr5:g.112842666T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112842666T>A , CM000667.2:g.112842666T>A	GRCh38
NC_000005.9:g.112178363T>A , CM000667.1:g.112178363T>A	GRCh37
NC_000005.8:g.112206262T>A	NCBI36
NG_008481.4:g.155146T>A , LRG_130:g.155146T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7126T>A	ENSP00000473355.2:p.Ser2376Thr
ENST00000505350.2:c.*7078T>A	ENSP00000481752.1:n.*7078T>A
ENST00000507379.6:c.7018T>A	ENSP00000423224.2:p.Ser2340Thr
ENST00000509732.6:c.7072T>A	ENSP00000426541.2:p.Ser2358Thr
ENST00000512211.7:c.7072T>A	ENSP00000423828.3:p.Ser2358Thr
ENST00000257430.9:c.7072T>A MANE Select	ENSP00000257430.4:p.Ser2358Thr
ENST00000257430.8:c.7072T>A	ENSP00000257430.4:p.Ser2358Thr
ENST00000508376.6:c.7072T>A	ENSP00000427089.2:p.Ser2358Thr
ENST00000508624.5:c.*6394T>A	ENSP00000424265.1:n.*6394T>A
ENST00000520401.1:c.230+13694T>A
NM_000038.5:c.7072T>A	NP_000029.2:p.Ser2358Thr
NM_001127510.2:c.7072T>A	NP_001120982.1:p.Ser2358Thr
NM_001127511.2:c.7018T>A	NP_001120983.2:p.Ser2340Thr
NM_001354895.1:c.7072T>A	NP_001341824.1:p.Ser2358Thr
NM_001354896.1:c.7126T>A	NP_001341825.1:p.Ser2376Thr
NM_001354897.1:c.7102T>A	NP_001341826.1:p.Ser2368Thr
NM_001354898.1:c.6997T>A	NP_001341827.1:p.Ser2333Thr
NM_001354899.1:c.6988T>A	NP_001341828.1:p.Ser2330Thr
NM_001354900.1:c.6949T>A	NP_001341829.1:p.Ser2317Thr
NM_001354901.1:c.6895T>A	NP_001341830.1:p.Ser2299Thr
NM_001354902.1:c.6799T>A	NP_001341831.1:p.Ser2267Thr
NM_001354903.1:c.6769T>A	NP_001341832.1:p.Ser2257Thr
NM_001354904.1:c.6694T>A	NP_001341833.1:p.Ser2232Thr
NM_001354905.1:c.6592T>A	NP_001341834.1:p.Ser2198Thr
NM_001354906.1:c.6223T>A	NP_001341835.1:p.Ser2075Thr
NM_000038.6:c.7072T>A MANE Select	NP_000029.2:p.Ser2358Thr
NM_001127510.3:c.7072T>A	NP_001120982.1:p.Ser2358Thr
NM_001127511.3:c.7018T>A	NP_001120983.2:p.Ser2340Thr
NM_001354895.2:c.7072T>A	NP_001341824.1:p.Ser2358Thr
NM_001354896.2:c.7126T>A	NP_001341825.1:p.Ser2376Thr
NM_001354897.2:c.7102T>A	NP_001341826.1:p.Ser2368Thr
NM_001354898.2:c.6997T>A	NP_001341827.1:p.Ser2333Thr
NM_001354899.2:c.6988T>A	NP_001341828.1:p.Ser2330Thr
NM_001354900.2:c.6949T>A	NP_001341829.1:p.Ser2317Thr
NM_001354901.2:c.6895T>A	NP_001341830.1:p.Ser2299Thr
NM_001354902.2:c.6799T>A	NP_001341831.1:p.Ser2267Thr
NM_001354903.2:c.6769T>A	NP_001341832.1:p.Ser2257Thr
NM_001354904.2:c.6694T>A	NP_001341833.1:p.Ser2232Thr
NM_001354905.2:c.6592T>A	NP_001341834.1:p.Ser2198Thr
NM_001354906.2:c.6223T>A	NP_001341835.1:p.Ser2075Thr