Canonical Allele Identifier: CA2674856343
Gene: APC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112828715_112828716insG , CM000667.2:g.112828715_112828716insG GRCh38
NC_000005.9:g.112164412_112164413insG , CM000667.1:g.112164412_112164413insG GRCh37
NC_000005.8:g.112192311_112192312insG NCBI36
NG_008481.4:g.141195_141196insG , LRG_130:g.141195_141196insG

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.1409-6236_1409-6235insG ENSP00000484935.2:n.1409-6236_1409-6235in...
ENST00000504915.3:c.1681-141_1681-140insG ENSP00000473355.2:n.1681-141_1681-140insG...
ENST00000505084.2:n.1683-141_1683-140insG
ENST00000505350.2:c.*1633-141_*1633-140insG ENSP00000481752.1:n.*1633-141_*1633-140in...
ENST00000507379.6:c.1573-141_1573-140insG ENSP00000423224.2:n.1573-141_1573-140insG...
ENST00000509732.6:c.1627-141_1627-140insG ENSP00000426541.2:n.1627-141_1627-140insG...
ENST00000512211.7:c.1627-141_1627-140insG ENSP00000423828.3:n.1627-141_1627-140insG...
ENST00000257430.9:c.1627-141_1627-140insG MANE Select ENSP00000257430.4:n.1627-141_1627-140insG...
ENST00000257430.8:c.1627-141_1627-140insG ENSP00000257430.4:n.1627-141_1627-140insG...
ENST00000502371.2:c.97-6236_97-6235insG
ENST00000504915.2:c.316-141_316-140insG ENSP00000473355.1:n.316-141_316-140insG
ENST00000505084.1:n.114-141_114-140insG
ENST00000507379.5:c.1573-141_1573-140insG ENSP00000423224.1:n.1573-141_1573-140insG...
ENST00000508376.6:c.1627-141_1627-140insG ENSP00000427089.2:n.1627-141_1627-140insG...
ENST00000508624.5:c.*949-141_*949-140insG ENSP00000424265.1:n.*949-141_*949-140insG...
ENST00000512211.6:c.1627-141_1627-140insG ENSP00000423828.2:n.1627-141_1627-140insG...
ENST00000520401.1:c.114-141_114-140insG
NM_000038.5:c.1627-141_1627-140insG NP_000029.2:n.1627-141_1627-140insG
NM_001127510.2:c.1627-141_1627-140insG NP_001120982.1:n.1627-141_1627-140insG
NM_001127511.2:c.1573-141_1573-140insG NP_001120983.2:n.1573-141_1573-140insG
NM_001354895.1:c.1627-141_1627-140insG NP_001341824.1:n.1627-141_1627-140insG
NM_001354896.1:c.1681-141_1681-140insG NP_001341825.1:n.1681-141_1681-140insG
NM_001354897.1:c.1657-141_1657-140insG NP_001341826.1:n.1657-141_1657-140insG
NM_001354898.1:c.1552-141_1552-140insG NP_001341827.1:n.1552-141_1552-140insG
NM_001354899.1:c.1543-141_1543-140insG NP_001341828.1:n.1543-141_1543-140insG
NM_001354900.1:c.1504-141_1504-140insG NP_001341829.1:n.1504-141_1504-140insG
NM_001354901.1:c.1450-141_1450-140insG NP_001341830.1:n.1450-141_1450-140insG
NM_001354902.1:c.1354-141_1354-140insG NP_001341831.1:n.1354-141_1354-140insG
NM_001354903.1:c.1324-141_1324-140insG NP_001341832.1:n.1324-141_1324-140insG
NM_001354904.1:c.1249-141_1249-140insG NP_001341833.1:n.1249-141_1249-140insG
NM_001354905.1:c.1147-141_1147-140insG NP_001341834.1:n.1147-141_1147-140insG
NM_001354906.1:c.778-141_778-140insG NP_001341835.1:n.778-141_778-140insG
NM_000038.6:c.1627-141_1627-140insG MANE Select NP_000029.2:n.1627-141_1627-140insG
NM_001127510.3:c.1627-141_1627-140insG NP_001120982.1:n.1627-141_1627-140insG
NM_001127511.3:c.1573-141_1573-140insG NP_001120983.2:n.1573-141_1573-140insG
NM_001354895.2:c.1627-141_1627-140insG NP_001341824.1:n.1627-141_1627-140insG
NM_001354896.2:c.1681-141_1681-140insG NP_001341825.1:n.1681-141_1681-140insG
NM_001354897.2:c.1657-141_1657-140insG NP_001341826.1:n.1657-141_1657-140insG
NM_001354898.2:c.1552-141_1552-140insG NP_001341827.1:n.1552-141_1552-140insG
NM_001354899.2:c.1543-141_1543-140insG NP_001341828.1:n.1543-141_1543-140insG
NM_001354900.2:c.1504-141_1504-140insG NP_001341829.1:n.1504-141_1504-140insG
NM_001354901.2:c.1450-141_1450-140insG NP_001341830.1:n.1450-141_1450-140insG
NM_001354902.2:c.1354-141_1354-140insG NP_001341831.1:n.1354-141_1354-140insG
NM_001354903.2:c.1324-141_1324-140insG NP_001341832.1:n.1324-141_1324-140insG
NM_001354904.2:c.1249-141_1249-140insG NP_001341833.1:n.1249-141_1249-140insG
NM_001354905.2:c.1147-141_1147-140insG NP_001341834.1:n.1147-141_1147-140insG
NM_001354906.2:c.778-141_778-140insG NP_001341835.1:n.778-141_778-140insG