Canonical Allele Identifier: CA445964043

Gene: APC

Linked Data

• gnomAD v4: 5-112839614-T-G
• MyVariant Identifiers: chr5:g.112175311T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839614T>G , CM000667.2:g.112839614T>G	GRCh38
NC_000005.9:g.112175311T>G , CM000667.1:g.112175311T>G	GRCh37
NC_000005.8:g.112203210T>G	NCBI36
NG_008481.4:g.152094T>G , LRG_130:g.152094T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3685T>G	ENSP00000484935.2:n.3685T>G
ENST00000504915.3:c.4074T>G	ENSP00000473355.2:p.Ser1358=
ENST00000505350.2:c.*4026T>G	ENSP00000481752.1:n.*4026T>G
ENST00000507379.6:c.3966T>G	ENSP00000423224.2:p.Ser1322=
ENST00000509732.6:c.4020T>G	ENSP00000426541.2:p.Ser1340=
ENST00000512211.7:c.4020T>G	ENSP00000423828.3:p.Ser1340=
ENST00000257430.9:c.4020T>G MANE Select	ENSP00000257430.4:p.Ser1340=
ENST00000257430.8:c.4020T>G	ENSP00000257430.4:p.Ser1340=
ENST00000502371.2:c.2373T>G
ENST00000508376.6:c.4020T>G	ENSP00000427089.2:p.Ser1340=
ENST00000508624.5:c.*3342T>G	ENSP00000424265.1:n.*3342T>G
ENST00000520401.1:c.230+10642T>G
NM_000038.5:c.4020T>G	NP_000029.2:p.Ser1340=
NM_001127510.2:c.4020T>G	NP_001120982.1:p.Ser1340=
NM_001127511.2:c.3966T>G	NP_001120983.2:p.Ser1322=
NM_001354895.1:c.4020T>G	NP_001341824.1:p.Ser1340=
NM_001354896.1:c.4074T>G	NP_001341825.1:p.Ser1358=
NM_001354897.1:c.4050T>G	NP_001341826.1:p.Ser1350=
NM_001354898.1:c.3945T>G	NP_001341827.1:p.Ser1315=
NM_001354899.1:c.3936T>G	NP_001341828.1:p.Ser1312=
NM_001354900.1:c.3897T>G	NP_001341829.1:p.Ser1299=
NM_001354901.1:c.3843T>G	NP_001341830.1:p.Ser1281=
NM_001354902.1:c.3747T>G	NP_001341831.1:p.Ser1249=
NM_001354903.1:c.3717T>G	NP_001341832.1:p.Ser1239=
NM_001354904.1:c.3642T>G	NP_001341833.1:p.Ser1214=
NM_001354905.1:c.3540T>G	NP_001341834.1:p.Ser1180=
NM_001354906.1:c.3171T>G	NP_001341835.1:p.Ser1057=
NM_000038.6:c.4020T>G MANE Select	NP_000029.2:p.Ser1340=
NM_001127510.3:c.4020T>G	NP_001120982.1:p.Ser1340=
NM_001127511.3:c.3966T>G	NP_001120983.2:p.Ser1322=
NM_001354895.2:c.4020T>G	NP_001341824.1:p.Ser1340=
NM_001354896.2:c.4074T>G	NP_001341825.1:p.Ser1358=
NM_001354897.2:c.4050T>G	NP_001341826.1:p.Ser1350=
NM_001354898.2:c.3945T>G	NP_001341827.1:p.Ser1315=
NM_001354899.2:c.3936T>G	NP_001341828.1:p.Ser1312=
NM_001354900.2:c.3897T>G	NP_001341829.1:p.Ser1299=
NM_001354901.2:c.3843T>G	NP_001341830.1:p.Ser1281=
NM_001354902.2:c.3747T>G	NP_001341831.1:p.Ser1249=
NM_001354903.2:c.3717T>G	NP_001341832.1:p.Ser1239=
NM_001354904.2:c.3642T>G	NP_001341833.1:p.Ser1214=
NM_001354905.2:c.3540T>G	NP_001341834.1:p.Ser1180=
NM_001354906.2:c.3171T>G	NP_001341835.1:p.Ser1057=