Canonical Allele Identifier: CA2674868404

Gene: APC

Linked Data

• gnomAD v4: 5-112842685-TGTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112842686_112842688del , CM000667.2:g.112842686_112842688del	GRCh38
NC_000005.9:g.112178383_112178385del , CM000667.1:g.112178383_112178385del	GRCh37
NC_000005.8:g.112206282_112206284del	NCBI36
NG_008481.4:g.155166_155168del , LRG_130:g.155166_155168del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7146_7148del	ENSP00000473355.2:p.Met2382_Ser2383delinsIle
ENST00000505350.2:c.*7098_*7100del	ENSP00000481752.1:n.*7098_*7100del
ENST00000507379.6:c.7038_7040del	ENSP00000423224.2:p.Met2346_Ser2347delinsIle
ENST00000509732.6:c.7092_7094del	ENSP00000426541.2:p.Met2364_Ser2365delinsIle
ENST00000512211.7:c.7092_7094del	ENSP00000423828.3:p.Met2364_Ser2365delinsIle
ENST00000257430.9:c.7092_7094del MANE Select	ENSP00000257430.4:p.Met2364_Ser2365delinsIle
ENST00000257430.8:c.7092_7094del	ENSP00000257430.4:p.Met2364_Ser2365delinsIle
ENST00000508376.6:c.7092_7094del	ENSP00000427089.2:p.Met2364_Ser2365delinsIle
ENST00000508624.5:c.*6414_*6416del	ENSP00000424265.1:n.*6414_*6416del
ENST00000520401.1:c.230+13714_230+13716del
NM_000038.5:c.7092_7094del	NP_000029.2:p.Met2364_Ser2365delinsIle
NM_001127510.2:c.7092_7094del	NP_001120982.1:p.Met2364_Ser2365delinsIle
NM_001127511.2:c.7038_7040del	NP_001120983.2:p.Met2346_Ser2347delinsIle
NM_001354895.1:c.7092_7094del	NP_001341824.1:p.Met2364_Ser2365delinsIle
NM_001354896.1:c.7146_7148del	NP_001341825.1:p.Met2382_Ser2383delinsIle
NM_001354897.1:c.7122_7124del	NP_001341826.1:p.Met2374_Ser2375delinsIle
NM_001354898.1:c.7017_7019del	NP_001341827.1:p.Met2339_Ser2340delinsIle
NM_001354899.1:c.7008_7010del	NP_001341828.1:p.Met2336_Ser2337delinsIle
NM_001354900.1:c.6969_6971del	NP_001341829.1:p.Met2323_Ser2324delinsIle
NM_001354901.1:c.6915_6917del	NP_001341830.1:p.Met2305_Ser2306delinsIle
NM_001354902.1:c.6819_6821del	NP_001341831.1:p.Met2273_Ser2274delinsIle
NM_001354903.1:c.6789_6791del	NP_001341832.1:p.Met2263_Ser2264delinsIle
NM_001354904.1:c.6714_6716del	NP_001341833.1:p.Met2238_Ser2239delinsIle
NM_001354905.1:c.6612_6614del	NP_001341834.1:p.Met2204_Ser2205delinsIle
NM_001354906.1:c.6243_6245del	NP_001341835.1:p.Met2081_Ser2082delinsIle
NM_000038.6:c.7092_7094del MANE Select	NP_000029.2:p.Met2364_Ser2365delinsIle
NM_001127510.3:c.7092_7094del	NP_001120982.1:p.Met2364_Ser2365delinsIle
NM_001127511.3:c.7038_7040del	NP_001120983.2:p.Met2346_Ser2347delinsIle
NM_001354895.2:c.7092_7094del	NP_001341824.1:p.Met2364_Ser2365delinsIle
NM_001354896.2:c.7146_7148del	NP_001341825.1:p.Met2382_Ser2383delinsIle
NM_001354897.2:c.7122_7124del	NP_001341826.1:p.Met2374_Ser2375delinsIle
NM_001354898.2:c.7017_7019del	NP_001341827.1:p.Met2339_Ser2340delinsIle
NM_001354899.2:c.7008_7010del	NP_001341828.1:p.Met2336_Ser2337delinsIle
NM_001354900.2:c.6969_6971del	NP_001341829.1:p.Met2323_Ser2324delinsIle
NM_001354901.2:c.6915_6917del	NP_001341830.1:p.Met2305_Ser2306delinsIle
NM_001354902.2:c.6819_6821del	NP_001341831.1:p.Met2273_Ser2274delinsIle
NM_001354903.2:c.6789_6791del	NP_001341832.1:p.Met2263_Ser2264delinsIle
NM_001354904.2:c.6714_6716del	NP_001341833.1:p.Met2238_Ser2239delinsIle
NM_001354905.2:c.6612_6614del	NP_001341834.1:p.Met2204_Ser2205delinsIle
NM_001354906.2:c.6243_6245del	NP_001341835.1:p.Met2081_Ser2082delinsIle