Canonical Allele Identifier: CA16032476

Gene: APC

Linked Data

• ClinVar Variation Id: 1745303
• ClinVar RCV Id: RCV002351472
• dbSNP Id: rs1561597648
• MyVariant Identifiers: chr5:g.112176388G>T (hg19) ; chr5:g.112840691G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840691G>T , CM000667.2:g.112840691G>T	GRCh38
NC_000005.9:g.112176388G>T , CM000667.1:g.112176388G>T	GRCh37
NC_000005.8:g.112204287G>T	NCBI36
NG_008481.4:g.153171G>T , LRG_130:g.153171G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5151G>T	ENSP00000473355.2:p.Glu1717Asp
ENST00000505350.2:c.*5103G>T	ENSP00000481752.1:n.*5103G>T
ENST00000507379.6:c.5043G>T	ENSP00000423224.2:p.Glu1681Asp
ENST00000509732.6:c.5097G>T	ENSP00000426541.2:p.Glu1699Asp
ENST00000512211.7:c.5097G>T	ENSP00000423828.3:p.Glu1699Asp
ENST00000257430.9:c.5097G>T MANE Select	ENSP00000257430.4:p.Glu1699Asp
ENST00000257430.8:c.5097G>T	ENSP00000257430.4:p.Glu1699Asp
ENST00000508376.6:c.5097G>T	ENSP00000427089.2:p.Glu1699Asp
ENST00000508624.5:c.*4419G>T	ENSP00000424265.1:n.*4419G>T
ENST00000520401.1:c.230+11719G>T
NM_000038.5:c.5097G>T	NP_000029.2:p.Glu1699Asp
NM_001127510.2:c.5097G>T	NP_001120982.1:p.Glu1699Asp
NM_001127511.2:c.5043G>T	NP_001120983.2:p.Glu1681Asp
NM_001354895.1:c.5097G>T	NP_001341824.1:p.Glu1699Asp
NM_001354896.1:c.5151G>T	NP_001341825.1:p.Glu1717Asp
NM_001354897.1:c.5127G>T	NP_001341826.1:p.Glu1709Asp
NM_001354898.1:c.5022G>T	NP_001341827.1:p.Glu1674Asp
NM_001354899.1:c.5013G>T	NP_001341828.1:p.Glu1671Asp
NM_001354900.1:c.4974G>T	NP_001341829.1:p.Glu1658Asp
NM_001354901.1:c.4920G>T	NP_001341830.1:p.Glu1640Asp
NM_001354902.1:c.4824G>T	NP_001341831.1:p.Glu1608Asp
NM_001354903.1:c.4794G>T	NP_001341832.1:p.Glu1598Asp
NM_001354904.1:c.4719G>T	NP_001341833.1:p.Glu1573Asp
NM_001354905.1:c.4617G>T	NP_001341834.1:p.Glu1539Asp
NM_001354906.1:c.4248G>T	NP_001341835.1:p.Glu1416Asp
NM_000038.6:c.5097G>T MANE Select	NP_000029.2:p.Glu1699Asp
NM_001127510.3:c.5097G>T	NP_001120982.1:p.Glu1699Asp
NM_001127511.3:c.5043G>T	NP_001120983.2:p.Glu1681Asp
NM_001354895.2:c.5097G>T	NP_001341824.1:p.Glu1699Asp
NM_001354896.2:c.5151G>T	NP_001341825.1:p.Glu1717Asp
NM_001354897.2:c.5127G>T	NP_001341826.1:p.Glu1709Asp
NM_001354898.2:c.5022G>T	NP_001341827.1:p.Glu1674Asp
NM_001354899.2:c.5013G>T	NP_001341828.1:p.Glu1671Asp
NM_001354900.2:c.4974G>T	NP_001341829.1:p.Glu1658Asp
NM_001354901.2:c.4920G>T	NP_001341830.1:p.Glu1640Asp
NM_001354902.2:c.4824G>T	NP_001341831.1:p.Glu1608Asp
NM_001354903.2:c.4794G>T	NP_001341832.1:p.Glu1598Asp
NM_001354904.2:c.4719G>T	NP_001341833.1:p.Glu1573Asp
NM_001354905.2:c.4617G>T	NP_001341834.1:p.Glu1539Asp
NM_001354906.2:c.4248G>T	NP_001341835.1:p.Glu1416Asp