Canonical Allele Identifier: CA1080222005

Gene: APC

Linked Data

• gnomAD v3: 5-112828454-ATTT-A
• gnomAD v4: 5-112828454-ATTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828455_112828457del , CM000667.2:g.112828455_112828457del	GRCh38
NC_000005.9:g.112164152_112164154del , CM000667.1:g.112164152_112164154del	GRCh37
NC_000005.8:g.112192051_112192053del	NCBI36
NG_008481.4:g.140935_140937del , LRG_130:g.140935_140937del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1408+6464_1408+6466del	ENSP00000484935.2:n.1408+6464_1408+6466del
ENST00000504915.3:c.1681-401_1681-399del	ENSP00000473355.2:n.1681-401_1681-399del
ENST00000505084.2:n.1683-401_1683-399del
ENST00000505350.2:c.*1633-401_*1633-399del	ENSP00000481752.1:n.*1633-401_*1633-399del
ENST00000507379.6:c.1573-401_1573-399del	ENSP00000423224.2:n.1573-401_1573-399del
ENST00000509732.6:c.1627-401_1627-399del	ENSP00000426541.2:n.1627-401_1627-399del
ENST00000512211.7:c.1627-401_1627-399del	ENSP00000423828.3:n.1627-401_1627-399del
ENST00000257430.9:c.1627-401_1627-399del MANE Select	ENSP00000257430.4:n.1627-401_1627-399del
ENST00000257430.8:c.1627-401_1627-399del	ENSP00000257430.4:n.1627-401_1627-399del
ENST00000502371.2:c.96+6464_96+6466del
ENST00000504915.2:c.316-401_316-399del	ENSP00000473355.1:n.316-401_316-399del
ENST00000505084.1:n.114-401_114-399del
ENST00000507379.5:c.1573-401_1573-399del	ENSP00000423224.1:n.1573-401_1573-399del
ENST00000508376.6:c.1627-401_1627-399del	ENSP00000427089.2:n.1627-401_1627-399del
ENST00000508624.5:c.*949-401_*949-399del	ENSP00000424265.1:n.*949-401_*949-399del
ENST00000512211.6:c.1627-401_1627-399del	ENSP00000423828.2:n.1627-401_1627-399del
ENST00000520401.1:c.114-401_114-399del
NM_000038.5:c.1627-401_1627-399del	NP_000029.2:n.1627-401_1627-399del
NM_001127510.2:c.1627-401_1627-399del	NP_001120982.1:n.1627-401_1627-399del
NM_001127511.2:c.1573-401_1573-399del	NP_001120983.2:n.1573-401_1573-399del
NM_001354895.1:c.1627-401_1627-399del	NP_001341824.1:n.1627-401_1627-399del
NM_001354896.1:c.1681-401_1681-399del	NP_001341825.1:n.1681-401_1681-399del
NM_001354897.1:c.1657-401_1657-399del	NP_001341826.1:n.1657-401_1657-399del
NM_001354898.1:c.1552-401_1552-399del	NP_001341827.1:n.1552-401_1552-399del
NM_001354899.1:c.1543-401_1543-399del	NP_001341828.1:n.1543-401_1543-399del
NM_001354900.1:c.1504-401_1504-399del	NP_001341829.1:n.1504-401_1504-399del
NM_001354901.1:c.1450-401_1450-399del	NP_001341830.1:n.1450-401_1450-399del
NM_001354902.1:c.1354-401_1354-399del	NP_001341831.1:n.1354-401_1354-399del
NM_001354903.1:c.1324-401_1324-399del	NP_001341832.1:n.1324-401_1324-399del
NM_001354904.1:c.1249-401_1249-399del	NP_001341833.1:n.1249-401_1249-399del
NM_001354905.1:c.1147-401_1147-399del	NP_001341834.1:n.1147-401_1147-399del
NM_001354906.1:c.778-401_778-399del	NP_001341835.1:n.778-401_778-399del
NM_000038.6:c.1627-401_1627-399del MANE Select	NP_000029.2:n.1627-401_1627-399del
NM_001127510.3:c.1627-401_1627-399del	NP_001120982.1:n.1627-401_1627-399del
NM_001127511.3:c.1573-401_1573-399del	NP_001120983.2:n.1573-401_1573-399del
NM_001354895.2:c.1627-401_1627-399del	NP_001341824.1:n.1627-401_1627-399del
NM_001354896.2:c.1681-401_1681-399del	NP_001341825.1:n.1681-401_1681-399del
NM_001354897.2:c.1657-401_1657-399del	NP_001341826.1:n.1657-401_1657-399del
NM_001354898.2:c.1552-401_1552-399del	NP_001341827.1:n.1552-401_1552-399del
NM_001354899.2:c.1543-401_1543-399del	NP_001341828.1:n.1543-401_1543-399del
NM_001354900.2:c.1504-401_1504-399del	NP_001341829.1:n.1504-401_1504-399del
NM_001354901.2:c.1450-401_1450-399del	NP_001341830.1:n.1450-401_1450-399del
NM_001354902.2:c.1354-401_1354-399del	NP_001341831.1:n.1354-401_1354-399del
NM_001354903.2:c.1324-401_1324-399del	NP_001341832.1:n.1324-401_1324-399del
NM_001354904.2:c.1249-401_1249-399del	NP_001341833.1:n.1249-401_1249-399del
NM_001354905.2:c.1147-401_1147-399del	NP_001341834.1:n.1147-401_1147-399del
NM_001354906.2:c.778-401_778-399del	NP_001341835.1:n.778-401_778-399del