Canonical Allele Identifier: CA445960360

Gene: APC

Linked Data

• ClinVar Variation Id: 2452703
• ClinVar RCV Id: RCV003177477
• dbSNP Id: rs2149782704
• MyVariant Identifiers: chr5:g.112154950T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112819253T>G , CM000667.2:g.112819253T>G	GRCh38
NC_000005.9:g.112154950T>G , CM000667.1:g.112154950T>G	GRCh37
NC_000005.8:g.112182849T>G	NCBI36
NG_008481.4:g.131733T>G , LRG_130:g.131733T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1221T>G	ENSP00000484935.2:p.Leu407=
ENST00000504915.3:c.1221T>G	ENSP00000473355.2:p.Leu407=
ENST00000505084.2:n.1277T>G
ENST00000505350.2:c.*1227T>G	ENSP00000481752.1:n.*1227T>G
ENST00000507379.6:c.1167T>G	ENSP00000423224.2:p.Leu389=
ENST00000509732.6:c.1221T>G	ENSP00000426541.2:p.Leu407=
ENST00000512211.7:c.1221T>G	ENSP00000423828.3:p.Leu407=
ENST00000257430.9:c.1221T>G MANE Select	ENSP00000257430.4:p.Leu407=
ENST00000257430.8:c.1221T>G	ENSP00000257430.4:p.Leu407=
ENST00000507379.5:c.1167T>G	ENSP00000423224.1:p.Leu389=
ENST00000508376.6:c.1221T>G	ENSP00000427089.2:p.Leu407=
ENST00000508624.5:c.*543T>G	ENSP00000424265.1:n.*543T>G
ENST00000512211.6:c.1221T>G	ENSP00000423828.2:p.Leu407=
NM_000038.5:c.1221T>G	NP_000029.2:p.Leu407=
NM_001127510.2:c.1221T>G	NP_001120982.1:p.Leu407=
NM_001127511.2:c.1167T>G	NP_001120983.2:p.Leu389=
NM_001354895.1:c.1221T>G	NP_001341824.1:p.Leu407=
NM_001354896.1:c.1221T>G	NP_001341825.1:p.Leu407=
NM_001354897.1:c.1251T>G	NP_001341826.1:p.Leu417=
NM_001354898.1:c.1146T>G	NP_001341827.1:p.Leu382=
NM_001354899.1:c.1137T>G	NP_001341828.1:p.Leu379=
NM_001354900.1:c.1044T>G	NP_001341829.1:p.Leu348=
NM_001354901.1:c.1044T>G	NP_001341830.1:p.Leu348=
NM_001354902.1:c.964-16T>G	NP_001341831.1:n.964-16T>G
NM_001354903.1:c.934-16T>G	NP_001341832.1:n.934-16T>G
NM_001354904.1:c.859-16T>G	NP_001341833.1:n.859-16T>G
NM_001354905.1:c.757-16T>G	NP_001341834.1:n.757-16T>G
NM_001354906.1:c.372T>G	NP_001341835.1:p.Leu124=
NM_000038.6:c.1221T>G MANE Select	NP_000029.2:p.Leu407=
NM_001127510.3:c.1221T>G	NP_001120982.1:p.Leu407=
NM_001127511.3:c.1167T>G	NP_001120983.2:p.Leu389=
NM_001354895.2:c.1221T>G	NP_001341824.1:p.Leu407=
NM_001354896.2:c.1221T>G	NP_001341825.1:p.Leu407=
NM_001354897.2:c.1251T>G	NP_001341826.1:p.Leu417=
NM_001354898.2:c.1146T>G	NP_001341827.1:p.Leu382=
NM_001354899.2:c.1137T>G	NP_001341828.1:p.Leu379=
NM_001354900.2:c.1044T>G	NP_001341829.1:p.Leu348=
NM_001354901.2:c.1044T>G	NP_001341830.1:p.Leu348=
NM_001354902.2:c.964-16T>G	NP_001341831.1:n.964-16T>G
NM_001354903.2:c.934-16T>G	NP_001341832.1:n.934-16T>G
NM_001354904.2:c.859-16T>G	NP_001341833.1:n.859-16T>G
NM_001354905.2:c.757-16T>G	NP_001341834.1:n.757-16T>G
NM_001354906.2:c.372T>G	NP_001341835.1:p.Leu124=