Canonical Allele Identifier: CA16031631

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112175988A>T (hg19) ; chr5:g.112840291A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840291A>T , CM000667.2:g.112840291A>T	GRCh38
NC_000005.9:g.112175988A>T , CM000667.1:g.112175988A>T	GRCh37
NC_000005.8:g.112203887A>T	NCBI36
NG_008481.4:g.152771A>T , LRG_130:g.152771A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4751A>T	ENSP00000473355.2:p.Asp1584Val
ENST00000505350.2:c.*4703A>T	ENSP00000481752.1:n.*4703A>T
ENST00000507379.6:c.4643A>T	ENSP00000423224.2:p.Asp1548Val
ENST00000509732.6:c.4697A>T	ENSP00000426541.2:p.Asp1566Val
ENST00000512211.7:c.4697A>T	ENSP00000423828.3:p.Asp1566Val
ENST00000257430.9:c.4697A>T MANE Select	ENSP00000257430.4:p.Asp1566Val
ENST00000257430.8:c.4697A>T	ENSP00000257430.4:p.Asp1566Val
ENST00000508376.6:c.4697A>T	ENSP00000427089.2:p.Asp1566Val
ENST00000508624.5:c.*4019A>T	ENSP00000424265.1:n.*4019A>T
ENST00000520401.1:c.230+11319A>T
NM_000038.5:c.4697A>T	NP_000029.2:p.Asp1566Val
NM_001127510.2:c.4697A>T	NP_001120982.1:p.Asp1566Val
NM_001127511.2:c.4643A>T	NP_001120983.2:p.Asp1548Val
NM_001354895.1:c.4697A>T	NP_001341824.1:p.Asp1566Val
NM_001354896.1:c.4751A>T	NP_001341825.1:p.Asp1584Val
NM_001354897.1:c.4727A>T	NP_001341826.1:p.Asp1576Val
NM_001354898.1:c.4622A>T	NP_001341827.1:p.Asp1541Val
NM_001354899.1:c.4613A>T	NP_001341828.1:p.Asp1538Val
NM_001354900.1:c.4574A>T	NP_001341829.1:p.Asp1525Val
NM_001354901.1:c.4520A>T	NP_001341830.1:p.Asp1507Val
NM_001354902.1:c.4424A>T	NP_001341831.1:p.Asp1475Val
NM_001354903.1:c.4394A>T	NP_001341832.1:p.Asp1465Val
NM_001354904.1:c.4319A>T	NP_001341833.1:p.Asp1440Val
NM_001354905.1:c.4217A>T	NP_001341834.1:p.Asp1406Val
NM_001354906.1:c.3848A>T	NP_001341835.1:p.Asp1283Val
NM_000038.6:c.4697A>T MANE Select	NP_000029.2:p.Asp1566Val
NM_001127510.3:c.4697A>T	NP_001120982.1:p.Asp1566Val
NM_001127511.3:c.4643A>T	NP_001120983.2:p.Asp1548Val
NM_001354895.2:c.4697A>T	NP_001341824.1:p.Asp1566Val
NM_001354896.2:c.4751A>T	NP_001341825.1:p.Asp1584Val
NM_001354897.2:c.4727A>T	NP_001341826.1:p.Asp1576Val
NM_001354898.2:c.4622A>T	NP_001341827.1:p.Asp1541Val
NM_001354899.2:c.4613A>T	NP_001341828.1:p.Asp1538Val
NM_001354900.2:c.4574A>T	NP_001341829.1:p.Asp1525Val
NM_001354901.2:c.4520A>T	NP_001341830.1:p.Asp1507Val
NM_001354902.2:c.4424A>T	NP_001341831.1:p.Asp1475Val
NM_001354903.2:c.4394A>T	NP_001341832.1:p.Asp1465Val
NM_001354904.2:c.4319A>T	NP_001341833.1:p.Asp1440Val
NM_001354905.2:c.4217A>T	NP_001341834.1:p.Asp1406Val
NM_001354906.2:c.3848A>T	NP_001341835.1:p.Asp1283Val