Canonical Allele Identifier: CA1080221988

Gene: APC

Linked Data

• gnomAD v3: 5-112828436-TAG-T
• gnomAD v4: 5-112828436-TAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828437_112828438del , CM000667.2:g.112828437_112828438del	GRCh38
NC_000005.9:g.112164134_112164135del , CM000667.1:g.112164134_112164135del	GRCh37
NC_000005.8:g.112192033_112192034del	NCBI36
NG_008481.4:g.140917_140918del , LRG_130:g.140917_140918del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1408+6446_1408+6447del	ENSP00000484935.2:n.1408+6446_1408+6447del
ENST00000504915.3:c.1681-419_1681-418del	ENSP00000473355.2:n.1681-419_1681-418del
ENST00000505084.2:n.1683-419_1683-418del
ENST00000505350.2:c.*1633-419_*1633-418del	ENSP00000481752.1:n.*1633-419_*1633-418del
ENST00000507379.6:c.1573-419_1573-418del	ENSP00000423224.2:n.1573-419_1573-418del
ENST00000509732.6:c.1627-419_1627-418del	ENSP00000426541.2:n.1627-419_1627-418del
ENST00000512211.7:c.1627-419_1627-418del	ENSP00000423828.3:n.1627-419_1627-418del
ENST00000257430.9:c.1627-419_1627-418del MANE Select	ENSP00000257430.4:n.1627-419_1627-418del
ENST00000257430.8:c.1627-419_1627-418del	ENSP00000257430.4:n.1627-419_1627-418del
ENST00000502371.2:c.96+6446_96+6447del
ENST00000504915.2:c.316-419_316-418del	ENSP00000473355.1:n.316-419_316-418del
ENST00000505084.1:n.114-419_114-418del
ENST00000507379.5:c.1573-419_1573-418del	ENSP00000423224.1:n.1573-419_1573-418del
ENST00000508376.6:c.1627-419_1627-418del	ENSP00000427089.2:n.1627-419_1627-418del
ENST00000508624.5:c.*949-419_*949-418del	ENSP00000424265.1:n.*949-419_*949-418del
ENST00000512211.6:c.1627-419_1627-418del	ENSP00000423828.2:n.1627-419_1627-418del
ENST00000520401.1:c.114-419_114-418del
NM_000038.5:c.1627-419_1627-418del	NP_000029.2:n.1627-419_1627-418del
NM_001127510.2:c.1627-419_1627-418del	NP_001120982.1:n.1627-419_1627-418del
NM_001127511.2:c.1573-419_1573-418del	NP_001120983.2:n.1573-419_1573-418del
NM_001354895.1:c.1627-419_1627-418del	NP_001341824.1:n.1627-419_1627-418del
NM_001354896.1:c.1681-419_1681-418del	NP_001341825.1:n.1681-419_1681-418del
NM_001354897.1:c.1657-419_1657-418del	NP_001341826.1:n.1657-419_1657-418del
NM_001354898.1:c.1552-419_1552-418del	NP_001341827.1:n.1552-419_1552-418del
NM_001354899.1:c.1543-419_1543-418del	NP_001341828.1:n.1543-419_1543-418del
NM_001354900.1:c.1504-419_1504-418del	NP_001341829.1:n.1504-419_1504-418del
NM_001354901.1:c.1450-419_1450-418del	NP_001341830.1:n.1450-419_1450-418del
NM_001354902.1:c.1354-419_1354-418del	NP_001341831.1:n.1354-419_1354-418del
NM_001354903.1:c.1324-419_1324-418del	NP_001341832.1:n.1324-419_1324-418del
NM_001354904.1:c.1249-419_1249-418del	NP_001341833.1:n.1249-419_1249-418del
NM_001354905.1:c.1147-419_1147-418del	NP_001341834.1:n.1147-419_1147-418del
NM_001354906.1:c.778-419_778-418del	NP_001341835.1:n.778-419_778-418del
NM_000038.6:c.1627-419_1627-418del MANE Select	NP_000029.2:n.1627-419_1627-418del
NM_001127510.3:c.1627-419_1627-418del	NP_001120982.1:n.1627-419_1627-418del
NM_001127511.3:c.1573-419_1573-418del	NP_001120983.2:n.1573-419_1573-418del
NM_001354895.2:c.1627-419_1627-418del	NP_001341824.1:n.1627-419_1627-418del
NM_001354896.2:c.1681-419_1681-418del	NP_001341825.1:n.1681-419_1681-418del
NM_001354897.2:c.1657-419_1657-418del	NP_001341826.1:n.1657-419_1657-418del
NM_001354898.2:c.1552-419_1552-418del	NP_001341827.1:n.1552-419_1552-418del
NM_001354899.2:c.1543-419_1543-418del	NP_001341828.1:n.1543-419_1543-418del
NM_001354900.2:c.1504-419_1504-418del	NP_001341829.1:n.1504-419_1504-418del
NM_001354901.2:c.1450-419_1450-418del	NP_001341830.1:n.1450-419_1450-418del
NM_001354902.2:c.1354-419_1354-418del	NP_001341831.1:n.1354-419_1354-418del
NM_001354903.2:c.1324-419_1324-418del	NP_001341832.1:n.1324-419_1324-418del
NM_001354904.2:c.1249-419_1249-418del	NP_001341833.1:n.1249-419_1249-418del
NM_001354905.2:c.1147-419_1147-418del	NP_001341834.1:n.1147-419_1147-418del
NM_001354906.2:c.778-419_778-418del	NP_001341835.1:n.778-419_778-418del