Canonical Allele Identifier: CA1573472394

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843200_112843203delinsCCTT , CM000667.2:g.112843200_112843203delinsCCTT	GRCh38
NC_000005.9:g.112178897_112178900delinsCCTT , CM000667.1:g.112178897_112178900delinsCCTT	GRCh37
NC_000005.8:g.112206796_112206799delinsCCTT	NCBI36
NG_008481.4:g.155680_155683delinsCCTT , LRG_130:g.155680_155683delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7660_7663delinsCCTT	ENSP00000473355.2:p.Pro2554=
ENST00000505350.2:c.*7612_*7615delinsCCTT	ENSP00000481752.1:n.*7612_*7615delinsCCTT
ENST00000507379.6:c.7552_7555delinsCCTT	ENSP00000423224.2:p.Pro2518=
ENST00000509732.6:c.7606_7609delinsCCTT	ENSP00000426541.2:p.Pro2536=
ENST00000512211.7:c.7606_7609delinsCCTT	ENSP00000423828.3:p.Pro2536=
ENST00000257430.9:c.7606_7609delinsCCTT MANE Select	ENSP00000257430.4:p.Pro2536=
ENST00000257430.8:c.7606_7609delinsCCTT	ENSP00000257430.4:p.Pro2536=
ENST00000508376.6:c.7606_7609delinsCCTT	ENSP00000427089.2:p.Pro2536=
ENST00000520401.1:c.231-13449_231-13446delinsCCTT
NM_000038.5:c.7606_7609delinsCCTT	NP_000029.2:p.Pro2536=
NM_001127510.2:c.7606_7609delinsCCTT	NP_001120982.1:p.Pro2536=
NM_001127511.2:c.7552_7555delinsCCTT	NP_001120983.2:p.Pro2518=
NM_001354895.1:c.7606_7609delinsCCTT	NP_001341824.1:p.Pro2536=
NM_001354896.1:c.7660_7663delinsCCTT	NP_001341825.1:p.Pro2554=
NM_001354897.1:c.7636_7639delinsCCTT	NP_001341826.1:p.Pro2546=
NM_001354898.1:c.7531_7534delinsCCTT	NP_001341827.1:p.Pro2511=
NM_001354899.1:c.7522_7525delinsCCTT	NP_001341828.1:p.Pro2508=
NM_001354900.1:c.7483_7486delinsCCTT	NP_001341829.1:p.Pro2495=
NM_001354901.1:c.7429_7432delinsCCTT	NP_001341830.1:p.Pro2477=
NM_001354902.1:c.7333_7336delinsCCTT	NP_001341831.1:p.Pro2445=
NM_001354903.1:c.7303_7306delinsCCTT	NP_001341832.1:p.Pro2435=
NM_001354904.1:c.7228_7231delinsCCTT	NP_001341833.1:p.Pro2410=
NM_001354905.1:c.7126_7129delinsCCTT	NP_001341834.1:p.Pro2376=
NM_001354906.1:c.6757_6760delinsCCTT	NP_001341835.1:p.Pro2253=
NM_000038.6:c.7606_7609delinsCCTT MANE Select	NP_000029.2:p.Pro2536=
NM_001127510.3:c.7606_7609delinsCCTT	NP_001120982.1:p.Pro2536=
NM_001127511.3:c.7552_7555delinsCCTT	NP_001120983.2:p.Pro2518=
NM_001354895.2:c.7606_7609delinsCCTT	NP_001341824.1:p.Pro2536=
NM_001354896.2:c.7660_7663delinsCCTT	NP_001341825.1:p.Pro2554=
NM_001354897.2:c.7636_7639delinsCCTT	NP_001341826.1:p.Pro2546=
NM_001354898.2:c.7531_7534delinsCCTT	NP_001341827.1:p.Pro2511=
NM_001354899.2:c.7522_7525delinsCCTT	NP_001341828.1:p.Pro2508=
NM_001354900.2:c.7483_7486delinsCCTT	NP_001341829.1:p.Pro2495=
NM_001354901.2:c.7429_7432delinsCCTT	NP_001341830.1:p.Pro2477=
NM_001354902.2:c.7333_7336delinsCCTT	NP_001341831.1:p.Pro2445=
NM_001354903.2:c.7303_7306delinsCCTT	NP_001341832.1:p.Pro2435=
NM_001354904.2:c.7228_7231delinsCCTT	NP_001341833.1:p.Pro2410=
NM_001354905.2:c.7126_7129delinsCCTT	NP_001341834.1:p.Pro2376=
NM_001354906.2:c.6757_6760delinsCCTT	NP_001341835.1:p.Pro2253=