Canonical Allele Identifier: CA1573470665

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840262_112840270delinsTATTGATTC , CM000667.2:g.112840262_112840270delinsTATTGATTC	GRCh38
NC_000005.9:g.112175959_112175967delinsTATTGATTC , CM000667.1:g.112175959_112175967delinsTATTGATTC	GRCh37
NC_000005.8:g.112203858_112203866delinsTATTGATTC	NCBI36
NG_008481.4:g.152742_152750delinsTATTGATTC , LRG_130:g.152742_152750delinsTATTGATTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4722_4730delinsTATTGATTC	ENSP00000473355.2:p.Thr1574=
ENST00000505350.2:c.*4674_*4682delinsTATTGATTC	ENSP00000481752.1:n.*4674_*4682delinsTATTGATTC
ENST00000507379.6:c.4614_4622delinsTATTGATTC	ENSP00000423224.2:p.Thr1538=
ENST00000509732.6:c.4668_4676delinsTATTGATTC	ENSP00000426541.2:p.Thr1556=
ENST00000512211.7:c.4668_4676delinsTATTGATTC	ENSP00000423828.3:p.Thr1556=
ENST00000257430.9:c.4668_4676delinsTATTGATTC MANE Select	ENSP00000257430.4:p.Thr1556=
ENST00000257430.8:c.4668_4676delinsTATTGATTC	ENSP00000257430.4:p.Thr1556=
ENST00000508376.6:c.4668_4676delinsTATTGATTC	ENSP00000427089.2:p.Thr1556=
ENST00000508624.5:c.*3990_*3998delinsTATTGATTC	ENSP00000424265.1:n.*3990_*3998delinsTATTGATTC
ENST00000520401.1:c.230+11290_230+11298delinsTATTGATTC
NM_000038.5:c.4668_4676delinsTATTGATTC	NP_000029.2:p.Thr1556=
NM_001127510.2:c.4668_4676delinsTATTGATTC	NP_001120982.1:p.Thr1556=
NM_001127511.2:c.4614_4622delinsTATTGATTC	NP_001120983.2:p.Thr1538=
NM_001354895.1:c.4668_4676delinsTATTGATTC	NP_001341824.1:p.Thr1556=
NM_001354896.1:c.4722_4730delinsTATTGATTC	NP_001341825.1:p.Thr1574=
NM_001354897.1:c.4698_4706delinsTATTGATTC	NP_001341826.1:p.Thr1566=
NM_001354898.1:c.4593_4601delinsTATTGATTC	NP_001341827.1:p.Thr1531=
NM_001354899.1:c.4584_4592delinsTATTGATTC	NP_001341828.1:p.Thr1528=
NM_001354900.1:c.4545_4553delinsTATTGATTC	NP_001341829.1:p.Thr1515=
NM_001354901.1:c.4491_4499delinsTATTGATTC	NP_001341830.1:p.Thr1497=
NM_001354902.1:c.4395_4403delinsTATTGATTC	NP_001341831.1:p.Thr1465=
NM_001354903.1:c.4365_4373delinsTATTGATTC	NP_001341832.1:p.Thr1455=
NM_001354904.1:c.4290_4298delinsTATTGATTC	NP_001341833.1:p.Thr1430=
NM_001354905.1:c.4188_4196delinsTATTGATTC	NP_001341834.1:p.Thr1396=
NM_001354906.1:c.3819_3827delinsTATTGATTC	NP_001341835.1:p.Thr1273=
NM_000038.6:c.4668_4676delinsTATTGATTC MANE Select	NP_000029.2:p.Thr1556=
NM_001127510.3:c.4668_4676delinsTATTGATTC	NP_001120982.1:p.Thr1556=
NM_001127511.3:c.4614_4622delinsTATTGATTC	NP_001120983.2:p.Thr1538=
NM_001354895.2:c.4668_4676delinsTATTGATTC	NP_001341824.1:p.Thr1556=
NM_001354896.2:c.4722_4730delinsTATTGATTC	NP_001341825.1:p.Thr1574=
NM_001354897.2:c.4698_4706delinsTATTGATTC	NP_001341826.1:p.Thr1566=
NM_001354898.2:c.4593_4601delinsTATTGATTC	NP_001341827.1:p.Thr1531=
NM_001354899.2:c.4584_4592delinsTATTGATTC	NP_001341828.1:p.Thr1528=
NM_001354900.2:c.4545_4553delinsTATTGATTC	NP_001341829.1:p.Thr1515=
NM_001354901.2:c.4491_4499delinsTATTGATTC	NP_001341830.1:p.Thr1497=
NM_001354902.2:c.4395_4403delinsTATTGATTC	NP_001341831.1:p.Thr1465=
NM_001354903.2:c.4365_4373delinsTATTGATTC	NP_001341832.1:p.Thr1455=
NM_001354904.2:c.4290_4298delinsTATTGATTC	NP_001341833.1:p.Thr1430=
NM_001354905.2:c.4188_4196delinsTATTGATTC	NP_001341834.1:p.Thr1396=
NM_001354906.2:c.3819_3827delinsTATTGATTC	NP_001341835.1:p.Thr1273=