Canonical Allele Identifier: CA124977744
Gene: APC HGNC NCBI

Linked Data

dbSNP Id: rs983428503

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112828723A>G , CM000667.2:g.112828723A>G GRCh38
NC_000005.9:g.112164420A>G , CM000667.1:g.112164420A>G GRCh37
NC_000005.8:g.112192319A>G NCBI36
NG_008481.4:g.141203A>G , LRG_130:g.141203A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.1409-6228A>G ENSP00000484935.2:n.1409-6228A>G
ENST00000504915.3:c.1681-133A>G ENSP00000473355.2:n.1681-133A>G
ENST00000505084.2:n.1683-133A>G
ENST00000505350.2:c.*1633-133A>G ENSP00000481752.1:n.*1633-133A>G
ENST00000507379.6:c.1573-133A>G ENSP00000423224.2:n.1573-133A>G
ENST00000509732.6:c.1627-133A>G ENSP00000426541.2:n.1627-133A>G
ENST00000512211.7:c.1627-133A>G ENSP00000423828.3:n.1627-133A>G
ENST00000257430.9:c.1627-133A>G MANE Select ENSP00000257430.4:n.1627-133A>G
ENST00000257430.8:c.1627-133A>G ENSP00000257430.4:n.1627-133A>G
ENST00000502371.2:c.97-6228A>G
ENST00000504915.2:c.316-133A>G ENSP00000473355.1:n.316-133A>G
ENST00000505084.1:n.114-133A>G
ENST00000507379.5:c.1573-133A>G ENSP00000423224.1:n.1573-133A>G
ENST00000508376.6:c.1627-133A>G ENSP00000427089.2:n.1627-133A>G
ENST00000508624.5:c.*949-133A>G ENSP00000424265.1:n.*949-133A>G
ENST00000512211.6:c.1627-133A>G ENSP00000423828.2:n.1627-133A>G
ENST00000520401.1:c.114-133A>G
NM_000038.5:c.1627-133A>G NP_000029.2:n.1627-133A>G
NM_001127510.2:c.1627-133A>G NP_001120982.1:n.1627-133A>G
NM_001127511.2:c.1573-133A>G NP_001120983.2:n.1573-133A>G
NM_001354895.1:c.1627-133A>G NP_001341824.1:n.1627-133A>G
NM_001354896.1:c.1681-133A>G NP_001341825.1:n.1681-133A>G
NM_001354897.1:c.1657-133A>G NP_001341826.1:n.1657-133A>G
NM_001354898.1:c.1552-133A>G NP_001341827.1:n.1552-133A>G
NM_001354899.1:c.1543-133A>G NP_001341828.1:n.1543-133A>G
NM_001354900.1:c.1504-133A>G NP_001341829.1:n.1504-133A>G
NM_001354901.1:c.1450-133A>G NP_001341830.1:n.1450-133A>G
NM_001354902.1:c.1354-133A>G NP_001341831.1:n.1354-133A>G
NM_001354903.1:c.1324-133A>G NP_001341832.1:n.1324-133A>G
NM_001354904.1:c.1249-133A>G NP_001341833.1:n.1249-133A>G
NM_001354905.1:c.1147-133A>G NP_001341834.1:n.1147-133A>G
NM_001354906.1:c.778-133A>G NP_001341835.1:n.778-133A>G
NM_000038.6:c.1627-133A>G MANE Select NP_000029.2:n.1627-133A>G
NM_001127510.3:c.1627-133A>G NP_001120982.1:n.1627-133A>G
NM_001127511.3:c.1573-133A>G NP_001120983.2:n.1573-133A>G
NM_001354895.2:c.1627-133A>G NP_001341824.1:n.1627-133A>G
NM_001354896.2:c.1681-133A>G NP_001341825.1:n.1681-133A>G
NM_001354897.2:c.1657-133A>G NP_001341826.1:n.1657-133A>G
NM_001354898.2:c.1552-133A>G NP_001341827.1:n.1552-133A>G
NM_001354899.2:c.1543-133A>G NP_001341828.1:n.1543-133A>G
NM_001354900.2:c.1504-133A>G NP_001341829.1:n.1504-133A>G
NM_001354901.2:c.1450-133A>G NP_001341830.1:n.1450-133A>G
NM_001354902.2:c.1354-133A>G NP_001341831.1:n.1354-133A>G
NM_001354903.2:c.1324-133A>G NP_001341832.1:n.1324-133A>G
NM_001354904.2:c.1249-133A>G NP_001341833.1:n.1249-133A>G
NM_001354905.2:c.1147-133A>G NP_001341834.1:n.1147-133A>G
NM_001354906.2:c.778-133A>G NP_001341835.1:n.778-133A>G