Canonical Allele Identifier: CA336406

Gene: APC

Linked Data

• ClinVar Variation Id: 215566
• ClinVar RCV Id: RCV000775333 ; RCV003765266 ; RCV004020446
• dbSNP Id: rs863224283
• MyVariant Identifiers: chr5:g.112176271A>G (hg19) ; chr5:g.112840574A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840574A>G , CM000667.2:g.112840574A>G	GRCh38
NC_000005.9:g.112176271A>G , CM000667.1:g.112176271A>G	GRCh37
NC_000005.8:g.112204170A>G	NCBI36
NG_008481.4:g.153054A>G , LRG_130:g.153054A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5034A>G	ENSP00000473355.2:p.Leu1678=
ENST00000505350.2:c.*4986A>G	ENSP00000481752.1:n.*4986A>G
ENST00000507379.6:c.4926A>G	ENSP00000423224.2:p.Leu1642=
ENST00000509732.6:c.4980A>G	ENSP00000426541.2:p.Leu1660=
ENST00000512211.7:c.4980A>G	ENSP00000423828.3:p.Leu1660=
ENST00000257430.9:c.4980A>G MANE Select	ENSP00000257430.4:p.Leu1660=
ENST00000257430.8:c.4980A>G	ENSP00000257430.4:p.Leu1660=
ENST00000508376.6:c.4980A>G	ENSP00000427089.2:p.Leu1660=
ENST00000508624.5:c.*4302A>G	ENSP00000424265.1:n.*4302A>G
ENST00000520401.1:c.230+11602A>G
NM_000038.5:c.4980A>G	NP_000029.2:p.Leu1660=
NM_001127510.2:c.4980A>G	NP_001120982.1:p.Leu1660=
NM_001127511.2:c.4926A>G	NP_001120983.2:p.Leu1642=
NM_001354895.1:c.4980A>G	NP_001341824.1:p.Leu1660=
NM_001354896.1:c.5034A>G	NP_001341825.1:p.Leu1678=
NM_001354897.1:c.5010A>G	NP_001341826.1:p.Leu1670=
NM_001354898.1:c.4905A>G	NP_001341827.1:p.Leu1635=
NM_001354899.1:c.4896A>G	NP_001341828.1:p.Leu1632=
NM_001354900.1:c.4857A>G	NP_001341829.1:p.Leu1619=
NM_001354901.1:c.4803A>G	NP_001341830.1:p.Leu1601=
NM_001354902.1:c.4707A>G	NP_001341831.1:p.Leu1569=
NM_001354903.1:c.4677A>G	NP_001341832.1:p.Leu1559=
NM_001354904.1:c.4602A>G	NP_001341833.1:p.Leu1534=
NM_001354905.1:c.4500A>G	NP_001341834.1:p.Leu1500=
NM_001354906.1:c.4131A>G	NP_001341835.1:p.Leu1377=
NM_000038.6:c.4980A>G MANE Select	NP_000029.2:p.Leu1660=
NM_001127510.3:c.4980A>G	NP_001120982.1:p.Leu1660=
NM_001127511.3:c.4926A>G	NP_001120983.2:p.Leu1642=
NM_001354895.2:c.4980A>G	NP_001341824.1:p.Leu1660=
NM_001354896.2:c.5034A>G	NP_001341825.1:p.Leu1678=
NM_001354897.2:c.5010A>G	NP_001341826.1:p.Leu1670=
NM_001354898.2:c.4905A>G	NP_001341827.1:p.Leu1635=
NM_001354899.2:c.4896A>G	NP_001341828.1:p.Leu1632=
NM_001354900.2:c.4857A>G	NP_001341829.1:p.Leu1619=
NM_001354901.2:c.4803A>G	NP_001341830.1:p.Leu1601=
NM_001354902.2:c.4707A>G	NP_001341831.1:p.Leu1569=
NM_001354903.2:c.4677A>G	NP_001341832.1:p.Leu1559=
NM_001354904.2:c.4602A>G	NP_001341833.1:p.Leu1534=
NM_001354905.2:c.4500A>G	NP_001341834.1:p.Leu1500=
NM_001354906.2:c.4131A>G	NP_001341835.1:p.Leu1377=