Canonical Allele Identifier: CA1573466600

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112842671_112842672delinsAG , CM000667.2:g.112842671_112842672delinsAG	GRCh38
NC_000005.9:g.112178368_112178369delinsAG , CM000667.1:g.112178368_112178369delinsAG	GRCh37
NC_000005.8:g.112206267_112206268delinsAG	NCBI36
NG_008481.4:g.155151_155152delinsAG , LRG_130:g.155151_155152delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7131_7132delinsAG	ENSP00000473355.2:p.Ser2377=
ENST00000505350.2:c.*7083_*7084delinsAG	ENSP00000481752.1:n.*7083_*7084delinsAG
ENST00000507379.6:c.7023_7024delinsAG	ENSP00000423224.2:p.Ser2341=
ENST00000509732.6:c.7077_7078delinsAG	ENSP00000426541.2:p.Ser2359=
ENST00000512211.7:c.7077_7078delinsAG	ENSP00000423828.3:p.Ser2359=
ENST00000257430.9:c.7077_7078delinsAG MANE Select	ENSP00000257430.4:p.Ser2359=
ENST00000257430.8:c.7077_7078delinsAG	ENSP00000257430.4:p.Ser2359=
ENST00000508376.6:c.7077_7078delinsAG	ENSP00000427089.2:p.Ser2359=
ENST00000508624.5:c.*6399_*6400delinsAG	ENSP00000424265.1:n.*6399_*6400delinsAG
ENST00000520401.1:c.230+13699_230+13700delinsAG
NM_000038.5:c.7077_7078delinsAG	NP_000029.2:p.Ser2359=
NM_001127510.2:c.7077_7078delinsAG	NP_001120982.1:p.Ser2359=
NM_001127511.2:c.7023_7024delinsAG	NP_001120983.2:p.Ser2341=
NM_001354895.1:c.7077_7078delinsAG	NP_001341824.1:p.Ser2359=
NM_001354896.1:c.7131_7132delinsAG	NP_001341825.1:p.Ser2377=
NM_001354897.1:c.7107_7108delinsAG	NP_001341826.1:p.Ser2369=
NM_001354898.1:c.7002_7003delinsAG	NP_001341827.1:p.Ser2334=
NM_001354899.1:c.6993_6994delinsAG	NP_001341828.1:p.Ser2331=
NM_001354900.1:c.6954_6955delinsAG	NP_001341829.1:p.Ser2318=
NM_001354901.1:c.6900_6901delinsAG	NP_001341830.1:p.Ser2300=
NM_001354902.1:c.6804_6805delinsAG	NP_001341831.1:p.Ser2268=
NM_001354903.1:c.6774_6775delinsAG	NP_001341832.1:p.Ser2258=
NM_001354904.1:c.6699_6700delinsAG	NP_001341833.1:p.Ser2233=
NM_001354905.1:c.6597_6598delinsAG	NP_001341834.1:p.Ser2199=
NM_001354906.1:c.6228_6229delinsAG	NP_001341835.1:p.Ser2076=
NM_000038.6:c.7077_7078delinsAG MANE Select	NP_000029.2:p.Ser2359=
NM_001127510.3:c.7077_7078delinsAG	NP_001120982.1:p.Ser2359=
NM_001127511.3:c.7023_7024delinsAG	NP_001120983.2:p.Ser2341=
NM_001354895.2:c.7077_7078delinsAG	NP_001341824.1:p.Ser2359=
NM_001354896.2:c.7131_7132delinsAG	NP_001341825.1:p.Ser2377=
NM_001354897.2:c.7107_7108delinsAG	NP_001341826.1:p.Ser2369=
NM_001354898.2:c.7002_7003delinsAG	NP_001341827.1:p.Ser2334=
NM_001354899.2:c.6993_6994delinsAG	NP_001341828.1:p.Ser2331=
NM_001354900.2:c.6954_6955delinsAG	NP_001341829.1:p.Ser2318=
NM_001354901.2:c.6900_6901delinsAG	NP_001341830.1:p.Ser2300=
NM_001354902.2:c.6804_6805delinsAG	NP_001341831.1:p.Ser2268=
NM_001354903.2:c.6774_6775delinsAG	NP_001341832.1:p.Ser2258=
NM_001354904.2:c.6699_6700delinsAG	NP_001341833.1:p.Ser2233=
NM_001354905.2:c.6597_6598delinsAG	NP_001341834.1:p.Ser2199=
NM_001354906.2:c.6228_6229delinsAG	NP_001341835.1:p.Ser2076=