Canonical Allele Identifier: CA658683422

Gene: APC

Linked Data

• ClinVar Variation Id: 489459
• ClinVar RCV Id: RCV000579896
• dbSNP Id: rs1554086216

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840398_112840400delinsACA , CM000667.2:g.112840398_112840400delinsACA	GRCh38
NC_000005.9:g.112176095_112176097delinsACA , CM000667.1:g.112176095_112176097delinsACA	GRCh37
NC_000005.8:g.112203994_112203996delinsACA	NCBI36
NG_008481.4:g.152878_152880delinsACA , LRG_130:g.152878_152880delinsACA

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.4858_4860delinsACA	ENSP00000473355.2:p.Pro1620Thr
ENST00000505350.2:c.*4810_*4812delinsACA	ENSP00000481752.1:n.*4810_*4812delinsACA
ENST00000507379.6:c.4750_4752delinsACA	ENSP00000423224.2:p.Pro1584Thr
ENST00000509732.6:c.4804_4806delinsACA	ENSP00000426541.2:p.Pro1602Thr
ENST00000512211.7:c.4804_4806delinsACA	ENSP00000423828.3:p.Pro1602Thr
ENST00000257430.9:c.4804_4806delinsACA MANE Select	ENSP00000257430.4:p.Pro1602Thr
ENST00000257430.8:c.4804_4806delinsACA	ENSP00000257430.4:p.Pro1602Thr
ENST00000508376.6:c.4804_4806delinsACA	ENSP00000427089.2:p.Pro1602Thr
ENST00000508624.5:c.*4126_*4128delinsACA	ENSP00000424265.1:n.*4126_*4128delinsACA
ENST00000520401.1:c.230+11426_230+11428delinsACA
NM_000038.5:c.4804_4806delinsACA	NP_000029.2:p.Pro1602Thr
NM_001127510.2:c.4804_4806delinsACA	NP_001120982.1:p.Pro1602Thr
NM_001127511.2:c.4750_4752delinsACA	NP_001120983.2:p.Pro1584Thr
NM_001354895.1:c.4804_4806delinsACA	NP_001341824.1:p.Pro1602Thr
NM_001354896.1:c.4858_4860delinsACA	NP_001341825.1:p.Pro1620Thr
NM_001354897.1:c.4834_4836delinsACA	NP_001341826.1:p.Pro1612Thr
NM_001354898.1:c.4729_4731delinsACA	NP_001341827.1:p.Pro1577Thr
NM_001354899.1:c.4720_4722delinsACA	NP_001341828.1:p.Pro1574Thr
NM_001354900.1:c.4681_4683delinsACA	NP_001341829.1:p.Pro1561Thr
NM_001354901.1:c.4627_4629delinsACA	NP_001341830.1:p.Pro1543Thr
NM_001354902.1:c.4531_4533delinsACA	NP_001341831.1:p.Pro1511Thr
NM_001354903.1:c.4501_4503delinsACA	NP_001341832.1:p.Pro1501Thr
NM_001354904.1:c.4426_4428delinsACA	NP_001341833.1:p.Pro1476Thr
NM_001354905.1:c.4324_4326delinsACA	NP_001341834.1:p.Pro1442Thr
NM_001354906.1:c.3955_3957delinsACA	NP_001341835.1:p.Pro1319Thr
NM_000038.6:c.4804_4806delinsACA MANE Select	NP_000029.2:p.Pro1602Thr
NM_001127510.3:c.4804_4806delinsACA	NP_001120982.1:p.Pro1602Thr
NM_001127511.3:c.4750_4752delinsACA	NP_001120983.2:p.Pro1584Thr
NM_001354895.2:c.4804_4806delinsACA	NP_001341824.1:p.Pro1602Thr
NM_001354896.2:c.4858_4860delinsACA	NP_001341825.1:p.Pro1620Thr
NM_001354897.2:c.4834_4836delinsACA	NP_001341826.1:p.Pro1612Thr
NM_001354898.2:c.4729_4731delinsACA	NP_001341827.1:p.Pro1577Thr
NM_001354899.2:c.4720_4722delinsACA	NP_001341828.1:p.Pro1574Thr
NM_001354900.2:c.4681_4683delinsACA	NP_001341829.1:p.Pro1561Thr
NM_001354901.2:c.4627_4629delinsACA	NP_001341830.1:p.Pro1543Thr
NM_001354902.2:c.4531_4533delinsACA	NP_001341831.1:p.Pro1511Thr
NM_001354903.2:c.4501_4503delinsACA	NP_001341832.1:p.Pro1501Thr
NM_001354904.2:c.4426_4428delinsACA	NP_001341833.1:p.Pro1476Thr
NM_001354905.2:c.4324_4326delinsACA	NP_001341834.1:p.Pro1442Thr
NM_001354906.2:c.3955_3957delinsACA	NP_001341835.1:p.Pro1319Thr