Canonical Allele Identifier: CA16038457

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843476C>T , CM000667.2:g.112843476C>T	GRCh38
NC_000005.9:g.112179173C>T , CM000667.1:g.112179173C>T	GRCh37
NC_000005.8:g.112207072C>T	NCBI36
NG_008481.4:g.155956C>T , LRG_130:g.155956C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.7882C>T MANE Select	NP_000029.2:p.Gln2628Ter
ENST00000257430.9:c.7882C>T MANE Select	ENSP00000257430.4:p.Gln2628Ter
NM_000038.5:c.7882C>T	NP_000029.2:p.Gln2628Ter
NM_001127510.2:c.7882C>T	NP_001120982.1:p.Gln2628Ter
NM_001127510.3:c.7882C>T	NP_001120982.1:p.Gln2628Ter
NM_001127511.2:c.7828C>T	NP_001120983.2:p.Gln2610Ter
NM_001127511.3:c.7828C>T	NP_001120983.2:p.Gln2610Ter
NM_001354895.1:c.7882C>T	NP_001341824.1:p.Gln2628Ter
NM_001354895.2:c.7882C>T	NP_001341824.1:p.Gln2628Ter
NM_001354896.1:c.7936C>T	NP_001341825.1:p.Gln2646Ter
NM_001354896.2:c.7936C>T	NP_001341825.1:p.Gln2646Ter
NM_001354897.1:c.7912C>T	NP_001341826.1:p.Gln2638Ter
NM_001354897.2:c.7912C>T	NP_001341826.1:p.Gln2638Ter
NM_001354898.1:c.7807C>T	NP_001341827.1:p.Gln2603Ter
NM_001354898.2:c.7807C>T	NP_001341827.1:p.Gln2603Ter
NM_001354899.1:c.7798C>T	NP_001341828.1:p.Gln2600Ter
NM_001354899.2:c.7798C>T	NP_001341828.1:p.Gln2600Ter
NM_001354900.1:c.7759C>T	NP_001341829.1:p.Gln2587Ter
NM_001354900.2:c.7759C>T	NP_001341829.1:p.Gln2587Ter
NM_001354901.1:c.7705C>T	NP_001341830.1:p.Gln2569Ter
NM_001354901.2:c.7705C>T	NP_001341830.1:p.Gln2569Ter
NM_001354902.1:c.7609C>T	NP_001341831.1:p.Gln2537Ter
NM_001354902.2:c.7609C>T	NP_001341831.1:p.Gln2537Ter
NM_001354903.1:c.7579C>T	NP_001341832.1:p.Gln2527Ter
NM_001354903.2:c.7579C>T	NP_001341832.1:p.Gln2527Ter
NM_001354904.1:c.7504C>T	NP_001341833.1:p.Gln2502Ter
NM_001354904.2:c.7504C>T	NP_001341833.1:p.Gln2502Ter
NM_001354905.1:c.7402C>T	NP_001341834.1:p.Gln2468Ter
NM_001354905.2:c.7402C>T	NP_001341834.1:p.Gln2468Ter
NM_001354906.1:c.7033C>T	NP_001341835.1:p.Gln2345Ter
NM_001354906.2:c.7033C>T	NP_001341835.1:p.Gln2345Ter
ENST00000257430.8:c.7882C>T	ENSP00000257430.4:p.Gln2628Ter
ENST00000504915.3:c.7936C>T	ENSP00000473355.2:p.Gln2646Ter
ENST00000505350.2:c.*7888C>T	ENSP00000481752.1:n.*7888C>T
ENST00000507379.6:c.7828C>T	ENSP00000423224.2:p.Gln2610Ter
ENST00000508376.6:c.7882C>T	ENSP00000427089.2:p.Gln2628Ter
ENST00000509732.6:c.7882C>T	ENSP00000426541.2:p.Gln2628Ter
ENST00000512211.7:c.7882C>T	ENSP00000423828.3:p.Gln2628Ter
ENST00000520401.1:c.231-13173C>T