Canonical Allele Identifier: CA446211012

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112179304T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843607T>G , CM000667.2:g.112843607T>G	GRCh38
NC_000005.9:g.112179304T>G , CM000667.1:g.112179304T>G	GRCh37
NC_000005.8:g.112207203T>G	NCBI36
NG_008481.4:g.156087T>G , LRG_130:g.156087T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8067T>G	ENSP00000473355.2:p.Ser2689=
ENST00000505350.2:c.*8019T>G	ENSP00000481752.1:n.*8019T>G
ENST00000507379.6:c.7959T>G	ENSP00000423224.2:p.Ser2653=
ENST00000509732.6:c.8013T>G	ENSP00000426541.2:p.Ser2671=
ENST00000512211.7:c.8013T>G	ENSP00000423828.3:p.Ser2671=
ENST00000257430.9:c.8013T>G MANE Select	ENSP00000257430.4:p.Ser2671=
ENST00000257430.8:c.8013T>G	ENSP00000257430.4:p.Ser2671=
ENST00000508376.6:c.8013T>G	ENSP00000427089.2:p.Ser2671=
ENST00000520401.1:c.231-13042T>G
NM_000038.5:c.8013T>G	NP_000029.2:p.Ser2671=
NM_001127510.2:c.8013T>G	NP_001120982.1:p.Ser2671=
NM_001127511.2:c.7959T>G	NP_001120983.2:p.Ser2653=
NM_001354895.1:c.8013T>G	NP_001341824.1:p.Ser2671=
NM_001354896.1:c.8067T>G	NP_001341825.1:p.Ser2689=
NM_001354897.1:c.8043T>G	NP_001341826.1:p.Ser2681=
NM_001354898.1:c.7938T>G	NP_001341827.1:p.Ser2646=
NM_001354899.1:c.7929T>G	NP_001341828.1:p.Ser2643=
NM_001354900.1:c.7890T>G	NP_001341829.1:p.Ser2630=
NM_001354901.1:c.7836T>G	NP_001341830.1:p.Ser2612=
NM_001354902.1:c.7740T>G	NP_001341831.1:p.Ser2580=
NM_001354903.1:c.7710T>G	NP_001341832.1:p.Ser2570=
NM_001354904.1:c.7635T>G	NP_001341833.1:p.Ser2545=
NM_001354905.1:c.7533T>G	NP_001341834.1:p.Ser2511=
NM_001354906.1:c.7164T>G	NP_001341835.1:p.Ser2388=
NM_000038.6:c.8013T>G MANE Select	NP_000029.2:p.Ser2671=
NM_001127510.3:c.8013T>G	NP_001120982.1:p.Ser2671=
NM_001127511.3:c.7959T>G	NP_001120983.2:p.Ser2653=
NM_001354895.2:c.8013T>G	NP_001341824.1:p.Ser2671=
NM_001354896.2:c.8067T>G	NP_001341825.1:p.Ser2689=
NM_001354897.2:c.8043T>G	NP_001341826.1:p.Ser2681=
NM_001354898.2:c.7938T>G	NP_001341827.1:p.Ser2646=
NM_001354899.2:c.7929T>G	NP_001341828.1:p.Ser2643=
NM_001354900.2:c.7890T>G	NP_001341829.1:p.Ser2630=
NM_001354901.2:c.7836T>G	NP_001341830.1:p.Ser2612=
NM_001354902.2:c.7740T>G	NP_001341831.1:p.Ser2580=
NM_001354903.2:c.7710T>G	NP_001341832.1:p.Ser2570=
NM_001354904.2:c.7635T>G	NP_001341833.1:p.Ser2545=
NM_001354905.2:c.7533T>G	NP_001341834.1:p.Ser2511=
NM_001354906.2:c.7164T>G	NP_001341835.1:p.Ser2388=