Canonical Allele Identifier: CA446209668

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112176553T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840856T>G , CM000667.2:g.112840856T>G	GRCh38
NC_000005.9:g.112176553T>G , CM000667.1:g.112176553T>G	GRCh37
NC_000005.8:g.112204452T>G	NCBI36
NG_008481.4:g.153336T>G , LRG_130:g.153336T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5316T>G	ENSP00000473355.2:p.Ser1772=
ENST00000505350.2:c.*5268T>G	ENSP00000481752.1:n.*5268T>G
ENST00000507379.6:c.5208T>G	ENSP00000423224.2:p.Ser1736=
ENST00000509732.6:c.5262T>G	ENSP00000426541.2:p.Ser1754=
ENST00000512211.7:c.5262T>G	ENSP00000423828.3:p.Ser1754=
ENST00000257430.9:c.5262T>G MANE Select	ENSP00000257430.4:p.Ser1754=
ENST00000257430.8:c.5262T>G	ENSP00000257430.4:p.Ser1754=
ENST00000508376.6:c.5262T>G	ENSP00000427089.2:p.Ser1754=
ENST00000508624.5:c.*4584T>G	ENSP00000424265.1:n.*4584T>G
ENST00000520401.1:c.230+11884T>G
NM_000038.5:c.5262T>G	NP_000029.2:p.Ser1754=
NM_001127510.2:c.5262T>G	NP_001120982.1:p.Ser1754=
NM_001127511.2:c.5208T>G	NP_001120983.2:p.Ser1736=
NM_001354895.1:c.5262T>G	NP_001341824.1:p.Ser1754=
NM_001354896.1:c.5316T>G	NP_001341825.1:p.Ser1772=
NM_001354897.1:c.5292T>G	NP_001341826.1:p.Ser1764=
NM_001354898.1:c.5187T>G	NP_001341827.1:p.Ser1729=
NM_001354899.1:c.5178T>G	NP_001341828.1:p.Ser1726=
NM_001354900.1:c.5139T>G	NP_001341829.1:p.Ser1713=
NM_001354901.1:c.5085T>G	NP_001341830.1:p.Ser1695=
NM_001354902.1:c.4989T>G	NP_001341831.1:p.Ser1663=
NM_001354903.1:c.4959T>G	NP_001341832.1:p.Ser1653=
NM_001354904.1:c.4884T>G	NP_001341833.1:p.Ser1628=
NM_001354905.1:c.4782T>G	NP_001341834.1:p.Ser1594=
NM_001354906.1:c.4413T>G	NP_001341835.1:p.Ser1471=
NM_000038.6:c.5262T>G MANE Select	NP_000029.2:p.Ser1754=
NM_001127510.3:c.5262T>G	NP_001120982.1:p.Ser1754=
NM_001127511.3:c.5208T>G	NP_001120983.2:p.Ser1736=
NM_001354895.2:c.5262T>G	NP_001341824.1:p.Ser1754=
NM_001354896.2:c.5316T>G	NP_001341825.1:p.Ser1772=
NM_001354897.2:c.5292T>G	NP_001341826.1:p.Ser1764=
NM_001354898.2:c.5187T>G	NP_001341827.1:p.Ser1729=
NM_001354899.2:c.5178T>G	NP_001341828.1:p.Ser1726=
NM_001354900.2:c.5139T>G	NP_001341829.1:p.Ser1713=
NM_001354901.2:c.5085T>G	NP_001341830.1:p.Ser1695=
NM_001354902.2:c.4989T>G	NP_001341831.1:p.Ser1663=
NM_001354903.2:c.4959T>G	NP_001341832.1:p.Ser1653=
NM_001354904.2:c.4884T>G	NP_001341833.1:p.Ser1628=
NM_001354905.2:c.4782T>G	NP_001341834.1:p.Ser1594=
NM_001354906.2:c.4413T>G	NP_001341835.1:p.Ser1471=