Canonical Allele Identifier: CA16037863

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112178900T>G (hg19) ; chr5:g.112843203T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843203T>G , CM000667.2:g.112843203T>G	GRCh38
NC_000005.9:g.112178900T>G , CM000667.1:g.112178900T>G	GRCh37
NC_000005.8:g.112206799T>G	NCBI36
NG_008481.4:g.155683T>G , LRG_130:g.155683T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7663T>G	ENSP00000473355.2:p.Ser2555Ala
ENST00000505350.2:c.*7615T>G	ENSP00000481752.1:n.*7615T>G
ENST00000507379.6:c.7555T>G	ENSP00000423224.2:p.Ser2519Ala
ENST00000509732.6:c.7609T>G	ENSP00000426541.2:p.Ser2537Ala
ENST00000512211.7:c.7609T>G	ENSP00000423828.3:p.Ser2537Ala
ENST00000257430.9:c.7609T>G MANE Select	ENSP00000257430.4:p.Ser2537Ala
ENST00000257430.8:c.7609T>G	ENSP00000257430.4:p.Ser2537Ala
ENST00000508376.6:c.7609T>G	ENSP00000427089.2:p.Ser2537Ala
ENST00000520401.1:c.231-13446T>G
NM_000038.5:c.7609T>G	NP_000029.2:p.Ser2537Ala
NM_001127510.2:c.7609T>G	NP_001120982.1:p.Ser2537Ala
NM_001127511.2:c.7555T>G	NP_001120983.2:p.Ser2519Ala
NM_001354895.1:c.7609T>G	NP_001341824.1:p.Ser2537Ala
NM_001354896.1:c.7663T>G	NP_001341825.1:p.Ser2555Ala
NM_001354897.1:c.7639T>G	NP_001341826.1:p.Ser2547Ala
NM_001354898.1:c.7534T>G	NP_001341827.1:p.Ser2512Ala
NM_001354899.1:c.7525T>G	NP_001341828.1:p.Ser2509Ala
NM_001354900.1:c.7486T>G	NP_001341829.1:p.Ser2496Ala
NM_001354901.1:c.7432T>G	NP_001341830.1:p.Ser2478Ala
NM_001354902.1:c.7336T>G	NP_001341831.1:p.Ser2446Ala
NM_001354903.1:c.7306T>G	NP_001341832.1:p.Ser2436Ala
NM_001354904.1:c.7231T>G	NP_001341833.1:p.Ser2411Ala
NM_001354905.1:c.7129T>G	NP_001341834.1:p.Ser2377Ala
NM_001354906.1:c.6760T>G	NP_001341835.1:p.Ser2254Ala
NM_000038.6:c.7609T>G MANE Select	NP_000029.2:p.Ser2537Ala
NM_001127510.3:c.7609T>G	NP_001120982.1:p.Ser2537Ala
NM_001127511.3:c.7555T>G	NP_001120983.2:p.Ser2519Ala
NM_001354895.2:c.7609T>G	NP_001341824.1:p.Ser2537Ala
NM_001354896.2:c.7663T>G	NP_001341825.1:p.Ser2555Ala
NM_001354897.2:c.7639T>G	NP_001341826.1:p.Ser2547Ala
NM_001354898.2:c.7534T>G	NP_001341827.1:p.Ser2512Ala
NM_001354899.2:c.7525T>G	NP_001341828.1:p.Ser2509Ala
NM_001354900.2:c.7486T>G	NP_001341829.1:p.Ser2496Ala
NM_001354901.2:c.7432T>G	NP_001341830.1:p.Ser2478Ala
NM_001354902.2:c.7336T>G	NP_001341831.1:p.Ser2446Ala
NM_001354903.2:c.7306T>G	NP_001341832.1:p.Ser2436Ala
NM_001354904.2:c.7231T>G	NP_001341833.1:p.Ser2411Ala
NM_001354905.2:c.7129T>G	NP_001341834.1:p.Ser2377Ala
NM_001354906.2:c.6760T>G	NP_001341835.1:p.Ser2254Ala