Canonical Allele Identifier: CA446210944

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843493T>C , CM000667.2:g.112843493T>C	GRCh38
NC_000005.9:g.112179190T>C , CM000667.1:g.112179190T>C	GRCh37
NC_000005.8:g.112207089T>C	NCBI36
NG_008481.4:g.155973T>C , LRG_130:g.155973T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.7899T>C MANE Select	NP_000029.2:p.Gly2633=
ENST00000257430.9:c.7899T>C MANE Select	ENSP00000257430.4:p.Gly2633=
NM_000038.5:c.7899T>C	NP_000029.2:p.Gly2633=
NM_001127510.2:c.7899T>C	NP_001120982.1:p.Gly2633=
NM_001127510.3:c.7899T>C	NP_001120982.1:p.Gly2633=
NM_001127511.2:c.7845T>C	NP_001120983.2:p.Gly2615=
NM_001127511.3:c.7845T>C	NP_001120983.2:p.Gly2615=
NM_001354895.1:c.7899T>C	NP_001341824.1:p.Gly2633=
NM_001354895.2:c.7899T>C	NP_001341824.1:p.Gly2633=
NM_001354896.1:c.7953T>C	NP_001341825.1:p.Gly2651=
NM_001354896.2:c.7953T>C	NP_001341825.1:p.Gly2651=
NM_001354897.1:c.7929T>C	NP_001341826.1:p.Gly2643=
NM_001354897.2:c.7929T>C	NP_001341826.1:p.Gly2643=
NM_001354898.1:c.7824T>C	NP_001341827.1:p.Gly2608=
NM_001354898.2:c.7824T>C	NP_001341827.1:p.Gly2608=
NM_001354899.1:c.7815T>C	NP_001341828.1:p.Gly2605=
NM_001354899.2:c.7815T>C	NP_001341828.1:p.Gly2605=
NM_001354900.1:c.7776T>C	NP_001341829.1:p.Gly2592=
NM_001354900.2:c.7776T>C	NP_001341829.1:p.Gly2592=
NM_001354901.1:c.7722T>C	NP_001341830.1:p.Gly2574=
NM_001354901.2:c.7722T>C	NP_001341830.1:p.Gly2574=
NM_001354902.1:c.7626T>C	NP_001341831.1:p.Gly2542=
NM_001354902.2:c.7626T>C	NP_001341831.1:p.Gly2542=
NM_001354903.1:c.7596T>C	NP_001341832.1:p.Gly2532=
NM_001354903.2:c.7596T>C	NP_001341832.1:p.Gly2532=
NM_001354904.1:c.7521T>C	NP_001341833.1:p.Gly2507=
NM_001354904.2:c.7521T>C	NP_001341833.1:p.Gly2507=
NM_001354905.1:c.7419T>C	NP_001341834.1:p.Gly2473=
NM_001354905.2:c.7419T>C	NP_001341834.1:p.Gly2473=
NM_001354906.1:c.7050T>C	NP_001341835.1:p.Gly2350=
NM_001354906.2:c.7050T>C	NP_001341835.1:p.Gly2350=
ENST00000257430.8:c.7899T>C	ENSP00000257430.4:p.Gly2633=
ENST00000504915.3:c.7953T>C	ENSP00000473355.2:p.Gly2651=
ENST00000505350.2:c.*7905T>C	ENSP00000481752.1:n.*7905T>C
ENST00000507379.6:c.7845T>C	ENSP00000423224.2:p.Gly2615=
ENST00000508376.6:c.7899T>C	ENSP00000427089.2:p.Gly2633=
ENST00000509732.6:c.7899T>C	ENSP00000426541.2:p.Gly2633=
ENST00000512211.7:c.7899T>C	ENSP00000423828.3:p.Gly2633=
ENST00000520401.1:c.231-13156T>C