Canonical Allele Identifier: CA446209593

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112176412T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840715T>G , CM000667.2:g.112840715T>G	GRCh38
NC_000005.9:g.112176412T>G , CM000667.1:g.112176412T>G	GRCh37
NC_000005.8:g.112204311T>G	NCBI36
NG_008481.4:g.153195T>G , LRG_130:g.153195T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5175T>G	ENSP00000473355.2:p.Ser1725=
ENST00000505350.2:c.*5127T>G	ENSP00000481752.1:n.*5127T>G
ENST00000507379.6:c.5067T>G	ENSP00000423224.2:p.Ser1689=
ENST00000509732.6:c.5121T>G	ENSP00000426541.2:p.Ser1707=
ENST00000512211.7:c.5121T>G	ENSP00000423828.3:p.Ser1707=
ENST00000257430.9:c.5121T>G MANE Select	ENSP00000257430.4:p.Ser1707=
ENST00000257430.8:c.5121T>G	ENSP00000257430.4:p.Ser1707=
ENST00000508376.6:c.5121T>G	ENSP00000427089.2:p.Ser1707=
ENST00000508624.5:c.*4443T>G	ENSP00000424265.1:n.*4443T>G
ENST00000520401.1:c.230+11743T>G
NM_000038.5:c.5121T>G	NP_000029.2:p.Ser1707=
NM_001127510.2:c.5121T>G	NP_001120982.1:p.Ser1707=
NM_001127511.2:c.5067T>G	NP_001120983.2:p.Ser1689=
NM_001354895.1:c.5121T>G	NP_001341824.1:p.Ser1707=
NM_001354896.1:c.5175T>G	NP_001341825.1:p.Ser1725=
NM_001354897.1:c.5151T>G	NP_001341826.1:p.Ser1717=
NM_001354898.1:c.5046T>G	NP_001341827.1:p.Ser1682=
NM_001354899.1:c.5037T>G	NP_001341828.1:p.Ser1679=
NM_001354900.1:c.4998T>G	NP_001341829.1:p.Ser1666=
NM_001354901.1:c.4944T>G	NP_001341830.1:p.Ser1648=
NM_001354902.1:c.4848T>G	NP_001341831.1:p.Ser1616=
NM_001354903.1:c.4818T>G	NP_001341832.1:p.Ser1606=
NM_001354904.1:c.4743T>G	NP_001341833.1:p.Ser1581=
NM_001354905.1:c.4641T>G	NP_001341834.1:p.Ser1547=
NM_001354906.1:c.4272T>G	NP_001341835.1:p.Ser1424=
NM_000038.6:c.5121T>G MANE Select	NP_000029.2:p.Ser1707=
NM_001127510.3:c.5121T>G	NP_001120982.1:p.Ser1707=
NM_001127511.3:c.5067T>G	NP_001120983.2:p.Ser1689=
NM_001354895.2:c.5121T>G	NP_001341824.1:p.Ser1707=
NM_001354896.2:c.5175T>G	NP_001341825.1:p.Ser1725=
NM_001354897.2:c.5151T>G	NP_001341826.1:p.Ser1717=
NM_001354898.2:c.5046T>G	NP_001341827.1:p.Ser1682=
NM_001354899.2:c.5037T>G	NP_001341828.1:p.Ser1679=
NM_001354900.2:c.4998T>G	NP_001341829.1:p.Ser1666=
NM_001354901.2:c.4944T>G	NP_001341830.1:p.Ser1648=
NM_001354902.2:c.4848T>G	NP_001341831.1:p.Ser1616=
NM_001354903.2:c.4818T>G	NP_001341832.1:p.Ser1606=
NM_001354904.2:c.4743T>G	NP_001341833.1:p.Ser1581=
NM_001354905.2:c.4641T>G	NP_001341834.1:p.Ser1547=
NM_001354906.2:c.4272T>G	NP_001341835.1:p.Ser1424=