Canonical Allele Identifier: CA1573473813

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840695_112840698delinsCAAG , CM000667.2:g.112840695_112840698delinsCAAG	GRCh38
NC_000005.9:g.112176392_112176395delinsCAAG , CM000667.1:g.112176392_112176395delinsCAAG	GRCh37
NC_000005.8:g.112204291_112204294delinsCAAG	NCBI36
NG_008481.4:g.153175_153178delinsCAAG , LRG_130:g.153175_153178delinsCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5155_5158delinsCAAG	ENSP00000473355.2:p.Gln1719=
ENST00000505350.2:c.*5107_*5110delinsCAAG	ENSP00000481752.1:n.*5107_*5110delinsCAAG
ENST00000507379.6:c.5047_5050delinsCAAG	ENSP00000423224.2:p.Gln1683=
ENST00000509732.6:c.5101_5104delinsCAAG	ENSP00000426541.2:p.Gln1701=
ENST00000512211.7:c.5101_5104delinsCAAG	ENSP00000423828.3:p.Gln1701=
ENST00000257430.9:c.5101_5104delinsCAAG MANE Select	ENSP00000257430.4:p.Gln1701=
ENST00000257430.8:c.5101_5104delinsCAAG	ENSP00000257430.4:p.Gln1701=
ENST00000508376.6:c.5101_5104delinsCAAG	ENSP00000427089.2:p.Gln1701=
ENST00000508624.5:c.*4423_*4426delinsCAAG	ENSP00000424265.1:n.*4423_*4426delinsCAAG
ENST00000520401.1:c.230+11723_230+11726delinsCAAG
NM_000038.5:c.5101_5104delinsCAAG	NP_000029.2:p.Gln1701=
NM_001127510.2:c.5101_5104delinsCAAG	NP_001120982.1:p.Gln1701=
NM_001127511.2:c.5047_5050delinsCAAG	NP_001120983.2:p.Gln1683=
NM_001354895.1:c.5101_5104delinsCAAG	NP_001341824.1:p.Gln1701=
NM_001354896.1:c.5155_5158delinsCAAG	NP_001341825.1:p.Gln1719=
NM_001354897.1:c.5131_5134delinsCAAG	NP_001341826.1:p.Gln1711=
NM_001354898.1:c.5026_5029delinsCAAG	NP_001341827.1:p.Gln1676=
NM_001354899.1:c.5017_5020delinsCAAG	NP_001341828.1:p.Gln1673=
NM_001354900.1:c.4978_4981delinsCAAG	NP_001341829.1:p.Gln1660=
NM_001354901.1:c.4924_4927delinsCAAG	NP_001341830.1:p.Gln1642=
NM_001354902.1:c.4828_4831delinsCAAG	NP_001341831.1:p.Gln1610=
NM_001354903.1:c.4798_4801delinsCAAG	NP_001341832.1:p.Gln1600=
NM_001354904.1:c.4723_4726delinsCAAG	NP_001341833.1:p.Gln1575=
NM_001354905.1:c.4621_4624delinsCAAG	NP_001341834.1:p.Gln1541=
NM_001354906.1:c.4252_4255delinsCAAG	NP_001341835.1:p.Gln1418=
NM_000038.6:c.5101_5104delinsCAAG MANE Select	NP_000029.2:p.Gln1701=
NM_001127510.3:c.5101_5104delinsCAAG	NP_001120982.1:p.Gln1701=
NM_001127511.3:c.5047_5050delinsCAAG	NP_001120983.2:p.Gln1683=
NM_001354895.2:c.5101_5104delinsCAAG	NP_001341824.1:p.Gln1701=
NM_001354896.2:c.5155_5158delinsCAAG	NP_001341825.1:p.Gln1719=
NM_001354897.2:c.5131_5134delinsCAAG	NP_001341826.1:p.Gln1711=
NM_001354898.2:c.5026_5029delinsCAAG	NP_001341827.1:p.Gln1676=
NM_001354899.2:c.5017_5020delinsCAAG	NP_001341828.1:p.Gln1673=
NM_001354900.2:c.4978_4981delinsCAAG	NP_001341829.1:p.Gln1660=
NM_001354901.2:c.4924_4927delinsCAAG	NP_001341830.1:p.Gln1642=
NM_001354902.2:c.4828_4831delinsCAAG	NP_001341831.1:p.Gln1610=
NM_001354903.2:c.4798_4801delinsCAAG	NP_001341832.1:p.Gln1600=
NM_001354904.2:c.4723_4726delinsCAAG	NP_001341833.1:p.Gln1575=
NM_001354905.2:c.4621_4624delinsCAAG	NP_001341834.1:p.Gln1541=
NM_001354906.2:c.4252_4255delinsCAAG	NP_001341835.1:p.Gln1418=