Canonical Allele Identifier: CA2674856348
Gene: APC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112828718_112828719insCTGG , CM000667.2:g.112828718_112828719insCTGG GRCh38
NC_000005.9:g.112164415_112164416insCTGG , CM000667.1:g.112164415_112164416insCTGG GRCh37
NC_000005.8:g.112192314_112192315insCTGG NCBI36
NG_008481.4:g.141198_141199insCTGG , LRG_130:g.141198_141199insCTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.1409-6233_1409-6232insCTGG ENSP00000484935.2:n.1409-6233_1409-6232in...
ENST00000504915.3:c.1681-138_1681-137insCTGG ENSP00000473355.2:n.1681-138_1681-137insC...
ENST00000505084.2:n.1683-138_1683-137insCTGG
ENST00000505350.2:c.*1633-138_*1633-137insCTGG ENSP00000481752.1:n.*1633-138_*1633-137in...
ENST00000507379.6:c.1573-138_1573-137insCTGG ENSP00000423224.2:n.1573-138_1573-137insC...
ENST00000509732.6:c.1627-138_1627-137insCTGG ENSP00000426541.2:n.1627-138_1627-137insC...
ENST00000512211.7:c.1627-138_1627-137insCTGG ENSP00000423828.3:n.1627-138_1627-137insC...
ENST00000257430.9:c.1627-138_1627-137insCTGG MANE Select ENSP00000257430.4:n.1627-138_1627-137insC...
ENST00000257430.8:c.1627-138_1627-137insCTGG ENSP00000257430.4:n.1627-138_1627-137insC...
ENST00000502371.2:c.97-6233_97-6232insCTGG
ENST00000504915.2:c.316-138_316-137insCTGG ENSP00000473355.1:n.316-138_316-137insCTG...
ENST00000505084.1:n.114-138_114-137insCTGG
ENST00000507379.5:c.1573-138_1573-137insCTGG ENSP00000423224.1:n.1573-138_1573-137insC...
ENST00000508376.6:c.1627-138_1627-137insCTGG ENSP00000427089.2:n.1627-138_1627-137insC...
ENST00000508624.5:c.*949-138_*949-137insCTGG ENSP00000424265.1:n.*949-138_*949-137insC...
ENST00000512211.6:c.1627-138_1627-137insCTGG ENSP00000423828.2:n.1627-138_1627-137insC...
ENST00000520401.1:c.114-138_114-137insCTGG
NM_000038.5:c.1627-138_1627-137insCTGG NP_000029.2:n.1627-138_1627-137insCTGG
NM_001127510.2:c.1627-138_1627-137insCTGG NP_001120982.1:n.1627-138_1627-137insCTGG...
NM_001127511.2:c.1573-138_1573-137insCTGG NP_001120983.2:n.1573-138_1573-137insCTGG...
NM_001354895.1:c.1627-138_1627-137insCTGG NP_001341824.1:n.1627-138_1627-137insCTGG...
NM_001354896.1:c.1681-138_1681-137insCTGG NP_001341825.1:n.1681-138_1681-137insCTGG...
NM_001354897.1:c.1657-138_1657-137insCTGG NP_001341826.1:n.1657-138_1657-137insCTGG...
NM_001354898.1:c.1552-138_1552-137insCTGG NP_001341827.1:n.1552-138_1552-137insCTGG...
NM_001354899.1:c.1543-138_1543-137insCTGG NP_001341828.1:n.1543-138_1543-137insCTGG...
NM_001354900.1:c.1504-138_1504-137insCTGG NP_001341829.1:n.1504-138_1504-137insCTGG...
NM_001354901.1:c.1450-138_1450-137insCTGG NP_001341830.1:n.1450-138_1450-137insCTGG...
NM_001354902.1:c.1354-138_1354-137insCTGG NP_001341831.1:n.1354-138_1354-137insCTGG...
NM_001354903.1:c.1324-138_1324-137insCTGG NP_001341832.1:n.1324-138_1324-137insCTGG...
NM_001354904.1:c.1249-138_1249-137insCTGG NP_001341833.1:n.1249-138_1249-137insCTGG...
NM_001354905.1:c.1147-138_1147-137insCTGG NP_001341834.1:n.1147-138_1147-137insCTGG...
NM_001354906.1:c.778-138_778-137insCTGG NP_001341835.1:n.778-138_778-137insCTGG
NM_000038.6:c.1627-138_1627-137insCTGG MANE Select NP_000029.2:n.1627-138_1627-137insCTGG
NM_001127510.3:c.1627-138_1627-137insCTGG NP_001120982.1:n.1627-138_1627-137insCTGG...
NM_001127511.3:c.1573-138_1573-137insCTGG NP_001120983.2:n.1573-138_1573-137insCTGG...
NM_001354895.2:c.1627-138_1627-137insCTGG NP_001341824.1:n.1627-138_1627-137insCTGG...
NM_001354896.2:c.1681-138_1681-137insCTGG NP_001341825.1:n.1681-138_1681-137insCTGG...
NM_001354897.2:c.1657-138_1657-137insCTGG NP_001341826.1:n.1657-138_1657-137insCTGG...
NM_001354898.2:c.1552-138_1552-137insCTGG NP_001341827.1:n.1552-138_1552-137insCTGG...
NM_001354899.2:c.1543-138_1543-137insCTGG NP_001341828.1:n.1543-138_1543-137insCTGG...
NM_001354900.2:c.1504-138_1504-137insCTGG NP_001341829.1:n.1504-138_1504-137insCTGG...
NM_001354901.2:c.1450-138_1450-137insCTGG NP_001341830.1:n.1450-138_1450-137insCTGG...
NM_001354902.2:c.1354-138_1354-137insCTGG NP_001341831.1:n.1354-138_1354-137insCTGG...
NM_001354903.2:c.1324-138_1324-137insCTGG NP_001341832.1:n.1324-138_1324-137insCTGG...
NM_001354904.2:c.1249-138_1249-137insCTGG NP_001341833.1:n.1249-138_1249-137insCTGG...
NM_001354905.2:c.1147-138_1147-137insCTGG NP_001341834.1:n.1147-138_1147-137insCTGG...
NM_001354906.2:c.778-138_778-137insCTGG NP_001341835.1:n.778-138_778-137insCTGG