Canonical Allele Identifier: CA10578361

Gene: APC

Linked Data

• ClinVar Variation Id: 231488
• ClinVar RCV Id: RCV000223153
• dbSNP Id: rs876659190
• MyVariant Identifiers: chr5:g.112175223T>G (hg19) ; chr5:g.112839526T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839526T>G , CM000667.2:g.112839526T>G	GRCh38
NC_000005.9:g.112175223T>G , CM000667.1:g.112175223T>G	GRCh37
NC_000005.8:g.112203122T>G	NCBI36
NG_008481.4:g.152006T>G , LRG_130:g.152006T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3597T>G	ENSP00000484935.2:n.3597T>G
ENST00000504915.3:c.3986T>G	ENSP00000473355.2:p.Ile1329Ser
ENST00000505350.2:c.*3938T>G	ENSP00000481752.1:n.*3938T>G
ENST00000507379.6:c.3878T>G	ENSP00000423224.2:p.Ile1293Ser
ENST00000509732.6:c.3932T>G	ENSP00000426541.2:p.Ile1311Ser
ENST00000512211.7:c.3932T>G	ENSP00000423828.3:p.Ile1311Ser
ENST00000257430.9:c.3932T>G MANE Select	ENSP00000257430.4:p.Ile1311Ser
ENST00000257430.8:c.3932T>G	ENSP00000257430.4:p.Ile1311Ser
ENST00000502371.2:c.2285T>G
ENST00000508376.6:c.3932T>G	ENSP00000427089.2:p.Ile1311Ser
ENST00000508624.5:c.*3254T>G	ENSP00000424265.1:n.*3254T>G
ENST00000520401.1:c.230+10554T>G
NM_000038.5:c.3932T>G	NP_000029.2:p.Ile1311Ser
NM_001127510.2:c.3932T>G	NP_001120982.1:p.Ile1311Ser
NM_001127511.2:c.3878T>G	NP_001120983.2:p.Ile1293Ser
NM_001354895.1:c.3932T>G	NP_001341824.1:p.Ile1311Ser
NM_001354896.1:c.3986T>G	NP_001341825.1:p.Ile1329Ser
NM_001354897.1:c.3962T>G	NP_001341826.1:p.Ile1321Ser
NM_001354898.1:c.3857T>G	NP_001341827.1:p.Ile1286Ser
NM_001354899.1:c.3848T>G	NP_001341828.1:p.Ile1283Ser
NM_001354900.1:c.3809T>G	NP_001341829.1:p.Ile1270Ser
NM_001354901.1:c.3755T>G	NP_001341830.1:p.Ile1252Ser
NM_001354902.1:c.3659T>G	NP_001341831.1:p.Ile1220Ser
NM_001354903.1:c.3629T>G	NP_001341832.1:p.Ile1210Ser
NM_001354904.1:c.3554T>G	NP_001341833.1:p.Ile1185Ser
NM_001354905.1:c.3452T>G	NP_001341834.1:p.Ile1151Ser
NM_001354906.1:c.3083T>G	NP_001341835.1:p.Ile1028Ser
NM_000038.6:c.3932T>G MANE Select	NP_000029.2:p.Ile1311Ser
NM_001127510.3:c.3932T>G	NP_001120982.1:p.Ile1311Ser
NM_001127511.3:c.3878T>G	NP_001120983.2:p.Ile1293Ser
NM_001354895.2:c.3932T>G	NP_001341824.1:p.Ile1311Ser
NM_001354896.2:c.3986T>G	NP_001341825.1:p.Ile1329Ser
NM_001354897.2:c.3962T>G	NP_001341826.1:p.Ile1321Ser
NM_001354898.2:c.3857T>G	NP_001341827.1:p.Ile1286Ser
NM_001354899.2:c.3848T>G	NP_001341828.1:p.Ile1283Ser
NM_001354900.2:c.3809T>G	NP_001341829.1:p.Ile1270Ser
NM_001354901.2:c.3755T>G	NP_001341830.1:p.Ile1252Ser
NM_001354902.2:c.3659T>G	NP_001341831.1:p.Ile1220Ser
NM_001354903.2:c.3629T>G	NP_001341832.1:p.Ile1210Ser
NM_001354904.2:c.3554T>G	NP_001341833.1:p.Ile1185Ser
NM_001354905.2:c.3452T>G	NP_001341834.1:p.Ile1151Ser
NM_001354906.2:c.3083T>G	NP_001341835.1:p.Ile1028Ser