Canonical Allele Identifier: CA445964001

Gene: APC

Linked Data

• dbSNP Id: rs772689871
• MyVariant Identifiers: chr5:g.112175029T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839332T>A , CM000667.2:g.112839332T>A	GRCh38
NC_000005.9:g.112175029T>A , CM000667.1:g.112175029T>A	GRCh37
NC_000005.8:g.112202928T>A	NCBI36
NG_008481.4:g.151812T>A , LRG_130:g.151812T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3403T>A	ENSP00000484935.2:n.3403T>A
ENST00000504915.3:c.3792T>A	ENSP00000473355.2:p.Ala1264=
ENST00000505350.2:c.*3744T>A	ENSP00000481752.1:n.*3744T>A
ENST00000507379.6:c.3684T>A	ENSP00000423224.2:p.Ala1228=
ENST00000509732.6:c.3738T>A	ENSP00000426541.2:p.Ala1246=
ENST00000512211.7:c.3738T>A	ENSP00000423828.3:p.Ala1246=
ENST00000257430.9:c.3738T>A MANE Select	ENSP00000257430.4:p.Ala1246=
ENST00000257430.8:c.3738T>A	ENSP00000257430.4:p.Ala1246=
ENST00000502371.2:c.2091T>A
ENST00000508376.6:c.3738T>A	ENSP00000427089.2:p.Ala1246=
ENST00000508624.5:c.*3060T>A	ENSP00000424265.1:n.*3060T>A
ENST00000512211.6:c.3738T>A	ENSP00000423828.2:p.Ala1246=
ENST00000520401.1:c.230+10360T>A
NM_000038.5:c.3738T>A	NP_000029.2:p.Ala1246=
NM_001127510.2:c.3738T>A	NP_001120982.1:p.Ala1246=
NM_001127511.2:c.3684T>A	NP_001120983.2:p.Ala1228=
NM_001354895.1:c.3738T>A	NP_001341824.1:p.Ala1246=
NM_001354896.1:c.3792T>A	NP_001341825.1:p.Ala1264=
NM_001354897.1:c.3768T>A	NP_001341826.1:p.Ala1256=
NM_001354898.1:c.3663T>A	NP_001341827.1:p.Ala1221=
NM_001354899.1:c.3654T>A	NP_001341828.1:p.Ala1218=
NM_001354900.1:c.3615T>A	NP_001341829.1:p.Ala1205=
NM_001354901.1:c.3561T>A	NP_001341830.1:p.Ala1187=
NM_001354902.1:c.3465T>A	NP_001341831.1:p.Ala1155=
NM_001354903.1:c.3435T>A	NP_001341832.1:p.Ala1145=
NM_001354904.1:c.3360T>A	NP_001341833.1:p.Ala1120=
NM_001354905.1:c.3258T>A	NP_001341834.1:p.Ala1086=
NM_001354906.1:c.2889T>A	NP_001341835.1:p.Ala963=
NM_000038.6:c.3738T>A MANE Select	NP_000029.2:p.Ala1246=
NM_001127510.3:c.3738T>A	NP_001120982.1:p.Ala1246=
NM_001127511.3:c.3684T>A	NP_001120983.2:p.Ala1228=
NM_001354895.2:c.3738T>A	NP_001341824.1:p.Ala1246=
NM_001354896.2:c.3792T>A	NP_001341825.1:p.Ala1264=
NM_001354897.2:c.3768T>A	NP_001341826.1:p.Ala1256=
NM_001354898.2:c.3663T>A	NP_001341827.1:p.Ala1221=
NM_001354899.2:c.3654T>A	NP_001341828.1:p.Ala1218=
NM_001354900.2:c.3615T>A	NP_001341829.1:p.Ala1205=
NM_001354901.2:c.3561T>A	NP_001341830.1:p.Ala1187=
NM_001354902.2:c.3465T>A	NP_001341831.1:p.Ala1155=
NM_001354903.2:c.3435T>A	NP_001341832.1:p.Ala1145=
NM_001354904.2:c.3360T>A	NP_001341833.1:p.Ala1120=
NM_001354905.2:c.3258T>A	NP_001341834.1:p.Ala1086=
NM_001354906.2:c.2889T>A	NP_001341835.1:p.Ala963=