Canonical Allele Identifier: CA124977662

Gene: APC

Linked Data

• dbSNP Id: rs906051429
• MyVariant Identifiers: chr5:g.112164166_112164167insG (hg19) ; chr5:g.112828469_112828470insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828469_112828470insG , CM000667.2:g.112828469_112828470insG	GRCh38
NC_000005.9:g.112164166_112164167insG , CM000667.1:g.112164166_112164167insG	GRCh37
NC_000005.8:g.112192065_112192066insG	NCBI36
NG_008481.4:g.140949_140950insG , LRG_130:g.140949_140950insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1408+6478_1408+6479insG	ENSP00000484935.2:n.1408+6478_1408+6479insG
ENST00000504915.3:c.1681-387_1681-386insG	ENSP00000473355.2:n.1681-387_1681-386insG
ENST00000505084.2:n.1683-387_1683-386insG
ENST00000505350.2:c.*1633-387_*1633-386insG	ENSP00000481752.1:n.*1633-387_*1633-386insG
ENST00000507379.6:c.1573-387_1573-386insG	ENSP00000423224.2:n.1573-387_1573-386insG
ENST00000509732.6:c.1627-387_1627-386insG	ENSP00000426541.2:n.1627-387_1627-386insG
ENST00000512211.7:c.1627-387_1627-386insG	ENSP00000423828.3:n.1627-387_1627-386insG
ENST00000257430.9:c.1627-387_1627-386insG MANE Select	ENSP00000257430.4:n.1627-387_1627-386insG
ENST00000257430.8:c.1627-387_1627-386insG	ENSP00000257430.4:n.1627-387_1627-386insG
ENST00000502371.2:c.96+6478_96+6479insG
ENST00000504915.2:c.316-387_316-386insG	ENSP00000473355.1:n.316-387_316-386insG
ENST00000505084.1:n.114-387_114-386insG
ENST00000507379.5:c.1573-387_1573-386insG	ENSP00000423224.1:n.1573-387_1573-386insG
ENST00000508376.6:c.1627-387_1627-386insG	ENSP00000427089.2:n.1627-387_1627-386insG
ENST00000508624.5:c.*949-387_*949-386insG	ENSP00000424265.1:n.*949-387_*949-386insG
ENST00000512211.6:c.1627-387_1627-386insG	ENSP00000423828.2:n.1627-387_1627-386insG
ENST00000520401.1:c.114-387_114-386insG
NM_000038.5:c.1627-387_1627-386insG	NP_000029.2:n.1627-387_1627-386insG
NM_001127510.2:c.1627-387_1627-386insG	NP_001120982.1:n.1627-387_1627-386insG
NM_001127511.2:c.1573-387_1573-386insG	NP_001120983.2:n.1573-387_1573-386insG
NM_001354895.1:c.1627-387_1627-386insG	NP_001341824.1:n.1627-387_1627-386insG
NM_001354896.1:c.1681-387_1681-386insG	NP_001341825.1:n.1681-387_1681-386insG
NM_001354897.1:c.1657-387_1657-386insG	NP_001341826.1:n.1657-387_1657-386insG
NM_001354898.1:c.1552-387_1552-386insG	NP_001341827.1:n.1552-387_1552-386insG
NM_001354899.1:c.1543-387_1543-386insG	NP_001341828.1:n.1543-387_1543-386insG
NM_001354900.1:c.1504-387_1504-386insG	NP_001341829.1:n.1504-387_1504-386insG
NM_001354901.1:c.1450-387_1450-386insG	NP_001341830.1:n.1450-387_1450-386insG
NM_001354902.1:c.1354-387_1354-386insG	NP_001341831.1:n.1354-387_1354-386insG
NM_001354903.1:c.1324-387_1324-386insG	NP_001341832.1:n.1324-387_1324-386insG
NM_001354904.1:c.1249-387_1249-386insG	NP_001341833.1:n.1249-387_1249-386insG
NM_001354905.1:c.1147-387_1147-386insG	NP_001341834.1:n.1147-387_1147-386insG
NM_001354906.1:c.778-387_778-386insG	NP_001341835.1:n.778-387_778-386insG
NM_000038.6:c.1627-387_1627-386insG MANE Select	NP_000029.2:n.1627-387_1627-386insG
NM_001127510.3:c.1627-387_1627-386insG	NP_001120982.1:n.1627-387_1627-386insG
NM_001127511.3:c.1573-387_1573-386insG	NP_001120983.2:n.1573-387_1573-386insG
NM_001354895.2:c.1627-387_1627-386insG	NP_001341824.1:n.1627-387_1627-386insG
NM_001354896.2:c.1681-387_1681-386insG	NP_001341825.1:n.1681-387_1681-386insG
NM_001354897.2:c.1657-387_1657-386insG	NP_001341826.1:n.1657-387_1657-386insG
NM_001354898.2:c.1552-387_1552-386insG	NP_001341827.1:n.1552-387_1552-386insG
NM_001354899.2:c.1543-387_1543-386insG	NP_001341828.1:n.1543-387_1543-386insG
NM_001354900.2:c.1504-387_1504-386insG	NP_001341829.1:n.1504-387_1504-386insG
NM_001354901.2:c.1450-387_1450-386insG	NP_001341830.1:n.1450-387_1450-386insG
NM_001354902.2:c.1354-387_1354-386insG	NP_001341831.1:n.1354-387_1354-386insG
NM_001354903.2:c.1324-387_1324-386insG	NP_001341832.1:n.1324-387_1324-386insG
NM_001354904.2:c.1249-387_1249-386insG	NP_001341833.1:n.1249-387_1249-386insG
NM_001354905.2:c.1147-387_1147-386insG	NP_001341834.1:n.1147-387_1147-386insG
NM_001354906.2:c.778-387_778-386insG	NP_001341835.1:n.778-387_778-386insG