Canonical Allele Identifier: CA561904933
Gene: APC HGNC NCBI

Linked Data

dbSNP Id: rs1250323678

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112828719_112828767dup , CM000667.2:g.112828719_112828767dup GRCh38
NC_000005.9:g.112164416_112164464dup , CM000667.1:g.112164416_112164464dup GRCh37
NC_000005.8:g.112192315_112192363dup NCBI36
NG_008481.4:g.141199_141247dup , LRG_130:g.141199_141247dup

Transcript Alleles

HGVS Amino-acid change
ENST00000257430.9:c.1627-137_1627-89dup MANE Select ENSP00000257430.4:n.1627-137_1627-89dup
ENST00000257430.8:c.1627-137_1627-89dup ENSP00000257430.4:n.1627-137_1627-89dup
ENST00000502371.2:n.97-6232_97-6184dup
ENST00000504915.2:n.316-137_316-89dup ENSP00000473355.1:n.316-137_316-89dup
ENST00000505084.1:n.114-137_114-89dup
ENST00000507379.5:c.1573-137_1573-89dup ENSP00000423224.1:n.1573-137_1573-89dup
ENST00000508376.6:c.1627-137_1627-89dup ENSP00000427089.2:n.1627-137_1627-89dup
ENST00000508624.5:c.*949-137_*949-89dup ENSP00000424265.1:n.*949-137_*949-89dup
ENST00000512211.6:c.1627-137_1627-89dup ENSP00000423828.2:n.1627-137_1627-89dup
ENST00000520401.1:n.114-137_114-89dup
NM_000038.5:c.1627-137_1627-89dup NP_000029.2:n.1627-137_1627-89dup
NM_001127510.2:c.1627-137_1627-89dup NP_001120982.1:n.1627-137_1627-89dup
NM_001127511.2:c.1573-137_1573-89dup NP_001120983.2:n.1573-137_1573-89dup
NM_001354895.1:c.1627-137_1627-89dup NP_001341824.1:n.1627-137_1627-89dup
NM_001354896.1:c.1681-137_1681-89dup NP_001341825.1:n.1681-137_1681-89dup
NM_001354897.1:c.1657-137_1657-89dup NP_001341826.1:n.1657-137_1657-89dup
NM_001354898.1:c.1552-137_1552-89dup NP_001341827.1:n.1552-137_1552-89dup
NM_001354899.1:c.1543-137_1543-89dup NP_001341828.1:n.1543-137_1543-89dup
NM_001354900.1:c.1504-137_1504-89dup NP_001341829.1:n.1504-137_1504-89dup
NM_001354901.1:c.1450-137_1450-89dup NP_001341830.1:n.1450-137_1450-89dup
NM_001354902.1:c.1354-137_1354-89dup NP_001341831.1:n.1354-137_1354-89dup
NM_001354903.1:c.1324-137_1324-89dup NP_001341832.1:n.1324-137_1324-89dup
NM_001354904.1:c.1249-137_1249-89dup NP_001341833.1:n.1249-137_1249-89dup
NM_001354905.1:c.1147-137_1147-89dup NP_001341834.1:n.1147-137_1147-89dup
NM_001354906.1:c.778-137_778-89dup NP_001341835.1:n.778-137_778-89dup
NM_000038.6:c.1627-137_1627-89dup MANE Select NP_000029.2:n.1627-137_1627-89dup
NM_001127510.3:c.1627-137_1627-89dup NP_001120982.1:n.1627-137_1627-89dup
NM_001127511.3:c.1573-137_1573-89dup NP_001120983.2:n.1573-137_1573-89dup
NM_001354895.2:c.1627-137_1627-89dup NP_001341824.1:n.1627-137_1627-89dup
NM_001354896.2:c.1681-137_1681-89dup NP_001341825.1:n.1681-137_1681-89dup
NM_001354897.2:c.1657-137_1657-89dup NP_001341826.1:n.1657-137_1657-89dup
NM_001354898.2:c.1552-137_1552-89dup NP_001341827.1:n.1552-137_1552-89dup
NM_001354899.2:c.1543-137_1543-89dup NP_001341828.1:n.1543-137_1543-89dup
NM_001354900.2:c.1504-137_1504-89dup NP_001341829.1:n.1504-137_1504-89dup
NM_001354901.2:c.1450-137_1450-89dup NP_001341830.1:n.1450-137_1450-89dup
NM_001354902.2:c.1354-137_1354-89dup NP_001341831.1:n.1354-137_1354-89dup
NM_001354903.2:c.1324-137_1324-89dup NP_001341832.1:n.1324-137_1324-89dup
NM_001354904.2:c.1249-137_1249-89dup NP_001341833.1:n.1249-137_1249-89dup
NM_001354905.2:c.1147-137_1147-89dup NP_001341834.1:n.1147-137_1147-89dup
NM_001354906.2:c.778-137_778-89dup NP_001341835.1:n.778-137_778-89dup