Canonical Allele Identifier: CA16036872

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112178426A>T (hg19) ; chr5:g.112842729A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112842729A>T , CM000667.2:g.112842729A>T	GRCh38
NC_000005.9:g.112178426A>T , CM000667.1:g.112178426A>T	GRCh37
NC_000005.8:g.112206325A>T	NCBI36
NG_008481.4:g.155209A>T , LRG_130:g.155209A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7189A>T	ENSP00000473355.2:p.Thr2397Ser
ENST00000505350.2:c.*7141A>T	ENSP00000481752.1:n.*7141A>T
ENST00000507379.6:c.7081A>T	ENSP00000423224.2:p.Thr2361Ser
ENST00000509732.6:c.7135A>T	ENSP00000426541.2:p.Thr2379Ser
ENST00000512211.7:c.7135A>T	ENSP00000423828.3:p.Thr2379Ser
ENST00000257430.9:c.7135A>T MANE Select	ENSP00000257430.4:p.Thr2379Ser
ENST00000257430.8:c.7135A>T	ENSP00000257430.4:p.Thr2379Ser
ENST00000508376.6:c.7135A>T	ENSP00000427089.2:p.Thr2379Ser
ENST00000508624.5:c.*6457A>T	ENSP00000424265.1:n.*6457A>T
ENST00000520401.1:c.230+13757A>T
NM_000038.5:c.7135A>T	NP_000029.2:p.Thr2379Ser
NM_001127510.2:c.7135A>T	NP_001120982.1:p.Thr2379Ser
NM_001127511.2:c.7081A>T	NP_001120983.2:p.Thr2361Ser
NM_001354895.1:c.7135A>T	NP_001341824.1:p.Thr2379Ser
NM_001354896.1:c.7189A>T	NP_001341825.1:p.Thr2397Ser
NM_001354897.1:c.7165A>T	NP_001341826.1:p.Thr2389Ser
NM_001354898.1:c.7060A>T	NP_001341827.1:p.Thr2354Ser
NM_001354899.1:c.7051A>T	NP_001341828.1:p.Thr2351Ser
NM_001354900.1:c.7012A>T	NP_001341829.1:p.Thr2338Ser
NM_001354901.1:c.6958A>T	NP_001341830.1:p.Thr2320Ser
NM_001354902.1:c.6862A>T	NP_001341831.1:p.Thr2288Ser
NM_001354903.1:c.6832A>T	NP_001341832.1:p.Thr2278Ser
NM_001354904.1:c.6757A>T	NP_001341833.1:p.Thr2253Ser
NM_001354905.1:c.6655A>T	NP_001341834.1:p.Thr2219Ser
NM_001354906.1:c.6286A>T	NP_001341835.1:p.Thr2096Ser
NM_000038.6:c.7135A>T MANE Select	NP_000029.2:p.Thr2379Ser
NM_001127510.3:c.7135A>T	NP_001120982.1:p.Thr2379Ser
NM_001127511.3:c.7081A>T	NP_001120983.2:p.Thr2361Ser
NM_001354895.2:c.7135A>T	NP_001341824.1:p.Thr2379Ser
NM_001354896.2:c.7189A>T	NP_001341825.1:p.Thr2397Ser
NM_001354897.2:c.7165A>T	NP_001341826.1:p.Thr2389Ser
NM_001354898.2:c.7060A>T	NP_001341827.1:p.Thr2354Ser
NM_001354899.2:c.7051A>T	NP_001341828.1:p.Thr2351Ser
NM_001354900.2:c.7012A>T	NP_001341829.1:p.Thr2338Ser
NM_001354901.2:c.6958A>T	NP_001341830.1:p.Thr2320Ser
NM_001354902.2:c.6862A>T	NP_001341831.1:p.Thr2288Ser
NM_001354903.2:c.6832A>T	NP_001341832.1:p.Thr2278Ser
NM_001354904.2:c.6757A>T	NP_001341833.1:p.Thr2253Ser
NM_001354905.2:c.6655A>T	NP_001341834.1:p.Thr2219Ser
NM_001354906.2:c.6286A>T	NP_001341835.1:p.Thr2096Ser