Canonical Allele Identifier: CA2695204933

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838980_112838993del , CM000667.2:g.112838980_112838993del	GRCh38
NC_000005.9:g.112174677_112174690del , CM000667.1:g.112174677_112174690del	GRCh37
NC_000005.8:g.112202576_112202589del	NCBI36
NG_008481.4:g.151460_151473del , LRG_130:g.151460_151473del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3051_3064del	ENSP00000484935.2:n.3051_3064del
ENST00000504915.3:c.3440_3453del	ENSP00000473355.2:p.Leu1147Ter
ENST00000505350.2:c.*3392_*3405del	ENSP00000481752.1:n.*3392_*3405del
ENST00000507379.6:c.3332_3345del	ENSP00000423224.2:p.Leu1111Ter
ENST00000509732.6:c.3386_3399del	ENSP00000426541.2:p.Leu1129Ter
ENST00000512211.7:c.3386_3399del	ENSP00000423828.3:p.Leu1129Ter
ENST00000257430.9:c.3386_3399del MANE Select	ENSP00000257430.4:p.Leu1129Ter
ENST00000257430.8:c.3386_3399del	ENSP00000257430.4:p.Leu1129Ter
ENST00000502371.2:c.1739_1752del
ENST00000507379.5:c.3332_3345del	ENSP00000423224.1:p.Leu1111Ter
ENST00000508376.6:c.3386_3399del	ENSP00000427089.2:p.Leu1129Ter
ENST00000508624.5:c.*2708_*2721del	ENSP00000424265.1:n.*2708_*2721del
ENST00000512211.6:c.3386_3399del	ENSP00000423828.2:p.Leu1129Ter
ENST00000520401.1:c.230+10008_230+10021del
NM_000038.5:c.3386_3399del	NP_000029.2:p.Leu1129Ter
NM_001127510.2:c.3386_3399del	NP_001120982.1:p.Leu1129Ter
NM_001127511.2:c.3332_3345del	NP_001120983.2:p.Leu1111Ter
NM_001354895.1:c.3386_3399del	NP_001341824.1:p.Leu1129Ter
NM_001354896.1:c.3440_3453del	NP_001341825.1:p.Leu1147Ter
NM_001354897.1:c.3416_3429del	NP_001341826.1:p.Leu1139Ter
NM_001354898.1:c.3311_3324del	NP_001341827.1:p.Leu1104Ter
NM_001354899.1:c.3302_3315del	NP_001341828.1:p.Leu1101Ter
NM_001354900.1:c.3263_3276del	NP_001341829.1:p.Leu1088Ter
NM_001354901.1:c.3209_3222del	NP_001341830.1:p.Leu1070Ter
NM_001354902.1:c.3113_3126del	NP_001341831.1:p.Leu1038Ter
NM_001354903.1:c.3083_3096del	NP_001341832.1:p.Leu1028Ter
NM_001354904.1:c.3008_3021del	NP_001341833.1:p.Leu1003Ter
NM_001354905.1:c.2906_2919del	NP_001341834.1:p.Leu969Ter
NM_001354906.1:c.2537_2550del	NP_001341835.1:p.Leu846Ter
NM_000038.6:c.3386_3399del MANE Select	NP_000029.2:p.Leu1129Ter
NM_001127510.3:c.3386_3399del	NP_001120982.1:p.Leu1129Ter
NM_001127511.3:c.3332_3345del	NP_001120983.2:p.Leu1111Ter
NM_001354895.2:c.3386_3399del	NP_001341824.1:p.Leu1129Ter
NM_001354896.2:c.3440_3453del	NP_001341825.1:p.Leu1147Ter
NM_001354897.2:c.3416_3429del	NP_001341826.1:p.Leu1139Ter
NM_001354898.2:c.3311_3324del	NP_001341827.1:p.Leu1104Ter
NM_001354899.2:c.3302_3315del	NP_001341828.1:p.Leu1101Ter
NM_001354900.2:c.3263_3276del	NP_001341829.1:p.Leu1088Ter
NM_001354901.2:c.3209_3222del	NP_001341830.1:p.Leu1070Ter
NM_001354902.2:c.3113_3126del	NP_001341831.1:p.Leu1038Ter
NM_001354903.2:c.3083_3096del	NP_001341832.1:p.Leu1028Ter
NM_001354904.2:c.3008_3021del	NP_001341833.1:p.Leu1003Ter
NM_001354905.2:c.2906_2919del	NP_001341834.1:p.Leu969Ter
NM_001354906.2:c.2537_2550del	NP_001341835.1:p.Leu846Ter