Canonical Allele Identifier: CA16025559

Gene: APC

Linked Data

• gnomAD v4: 5-112835149-A-G
• MyVariant Identifiers: chr5:g.112170846A>G (hg19) ; chr5:g.112835149A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835149A>G , CM000667.2:g.112835149A>G	GRCh38
NC_000005.9:g.112170846A>G , CM000667.1:g.112170846A>G	GRCh37
NC_000005.8:g.112198745A>G	NCBI36
NG_008481.4:g.147629A>G , LRG_130:g.147629A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1607A>G	ENSP00000484935.2:n.1607A>G
ENST00000504915.3:c.1996A>G	ENSP00000473355.2:p.Thr666Ala
ENST00000505350.2:c.*1948A>G	ENSP00000481752.1:n.*1948A>G
ENST00000507379.6:c.1888A>G	ENSP00000423224.2:p.Thr630Ala
ENST00000509732.6:c.1942A>G	ENSP00000426541.2:p.Thr648Ala
ENST00000512211.7:c.1942A>G	ENSP00000423828.3:p.Thr648Ala
ENST00000257430.9:c.1942A>G MANE Select	ENSP00000257430.4:p.Thr648Ala
ENST00000257430.8:c.1942A>G	ENSP00000257430.4:p.Thr648Ala
ENST00000502371.2:c.295A>G
ENST00000504915.2:c.631A>G	ENSP00000473355.1:p.Thr211Ala
ENST00000507379.5:c.1888A>G	ENSP00000423224.1:p.Thr630Ala
ENST00000508376.6:c.1942A>G	ENSP00000427089.2:p.Thr648Ala
ENST00000508624.5:c.*1264A>G	ENSP00000424265.1:n.*1264A>G
ENST00000512211.6:c.1942A>G	ENSP00000423828.2:p.Thr648Ala
ENST00000520401.1:c.230+6177A>G
NM_000038.5:c.1942A>G	NP_000029.2:p.Thr648Ala
NM_001127510.2:c.1942A>G	NP_001120982.1:p.Thr648Ala
NM_001127511.2:c.1888A>G	NP_001120983.2:p.Thr630Ala
NM_001354895.1:c.1942A>G	NP_001341824.1:p.Thr648Ala
NM_001354896.1:c.1996A>G	NP_001341825.1:p.Thr666Ala
NM_001354897.1:c.1972A>G	NP_001341826.1:p.Thr658Ala
NM_001354898.1:c.1867A>G	NP_001341827.1:p.Thr623Ala
NM_001354899.1:c.1858A>G	NP_001341828.1:p.Thr620Ala
NM_001354900.1:c.1819A>G	NP_001341829.1:p.Thr607Ala
NM_001354901.1:c.1765A>G	NP_001341830.1:p.Thr589Ala
NM_001354902.1:c.1669A>G	NP_001341831.1:p.Thr557Ala
NM_001354903.1:c.1639A>G	NP_001341832.1:p.Thr547Ala
NM_001354904.1:c.1564A>G	NP_001341833.1:p.Thr522Ala
NM_001354905.1:c.1462A>G	NP_001341834.1:p.Thr488Ala
NM_001354906.1:c.1093A>G	NP_001341835.1:p.Thr365Ala
NM_000038.6:c.1942A>G MANE Select	NP_000029.2:p.Thr648Ala
NM_001127510.3:c.1942A>G	NP_001120982.1:p.Thr648Ala
NM_001127511.3:c.1888A>G	NP_001120983.2:p.Thr630Ala
NM_001354895.2:c.1942A>G	NP_001341824.1:p.Thr648Ala
NM_001354896.2:c.1996A>G	NP_001341825.1:p.Thr666Ala
NM_001354897.2:c.1972A>G	NP_001341826.1:p.Thr658Ala
NM_001354898.2:c.1867A>G	NP_001341827.1:p.Thr623Ala
NM_001354899.2:c.1858A>G	NP_001341828.1:p.Thr620Ala
NM_001354900.2:c.1819A>G	NP_001341829.1:p.Thr607Ala
NM_001354901.2:c.1765A>G	NP_001341830.1:p.Thr589Ala
NM_001354902.2:c.1669A>G	NP_001341831.1:p.Thr557Ala
NM_001354903.2:c.1639A>G	NP_001341832.1:p.Thr547Ala
NM_001354904.2:c.1564A>G	NP_001341833.1:p.Thr522Ala
NM_001354905.2:c.1462A>G	NP_001341834.1:p.Thr488Ala
NM_001354906.2:c.1093A>G	NP_001341835.1:p.Thr365Ala