Canonical Allele Identifier: CA16038056

Gene: APC

Linked Data

• ClinVar Variation Id: 2452755
• ClinVar RCV Id: RCV003177529 ; RCV003745562
• dbSNP Id: rs2149992149
• gnomAD v4: 5-112843293-A-T
• MyVariant Identifiers: chr5:g.112178990A>T (hg19) ; chr5:g.112843293A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843293A>T , CM000667.2:g.112843293A>T	GRCh38
NC_000005.9:g.112178990A>T , CM000667.1:g.112178990A>T	GRCh37
NC_000005.8:g.112206889A>T	NCBI36
NG_008481.4:g.155773A>T , LRG_130:g.155773A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7753A>T	ENSP00000473355.2:p.Thr2585Ser
ENST00000505350.2:c.*7705A>T	ENSP00000481752.1:n.*7705A>T
ENST00000507379.6:c.7645A>T	ENSP00000423224.2:p.Thr2549Ser
ENST00000509732.6:c.7699A>T	ENSP00000426541.2:p.Thr2567Ser
ENST00000512211.7:c.7699A>T	ENSP00000423828.3:p.Thr2567Ser
ENST00000257430.9:c.7699A>T MANE Select	ENSP00000257430.4:p.Thr2567Ser
ENST00000257430.8:c.7699A>T	ENSP00000257430.4:p.Thr2567Ser
ENST00000508376.6:c.7699A>T	ENSP00000427089.2:p.Thr2567Ser
ENST00000520401.1:c.231-13356A>T
NM_000038.5:c.7699A>T	NP_000029.2:p.Thr2567Ser
NM_001127510.2:c.7699A>T	NP_001120982.1:p.Thr2567Ser
NM_001127511.2:c.7645A>T	NP_001120983.2:p.Thr2549Ser
NM_001354895.1:c.7699A>T	NP_001341824.1:p.Thr2567Ser
NM_001354896.1:c.7753A>T	NP_001341825.1:p.Thr2585Ser
NM_001354897.1:c.7729A>T	NP_001341826.1:p.Thr2577Ser
NM_001354898.1:c.7624A>T	NP_001341827.1:p.Thr2542Ser
NM_001354899.1:c.7615A>T	NP_001341828.1:p.Thr2539Ser
NM_001354900.1:c.7576A>T	NP_001341829.1:p.Thr2526Ser
NM_001354901.1:c.7522A>T	NP_001341830.1:p.Thr2508Ser
NM_001354902.1:c.7426A>T	NP_001341831.1:p.Thr2476Ser
NM_001354903.1:c.7396A>T	NP_001341832.1:p.Thr2466Ser
NM_001354904.1:c.7321A>T	NP_001341833.1:p.Thr2441Ser
NM_001354905.1:c.7219A>T	NP_001341834.1:p.Thr2407Ser
NM_001354906.1:c.6850A>T	NP_001341835.1:p.Thr2284Ser
NM_000038.6:c.7699A>T MANE Select	NP_000029.2:p.Thr2567Ser
NM_001127510.3:c.7699A>T	NP_001120982.1:p.Thr2567Ser
NM_001127511.3:c.7645A>T	NP_001120983.2:p.Thr2549Ser
NM_001354895.2:c.7699A>T	NP_001341824.1:p.Thr2567Ser
NM_001354896.2:c.7753A>T	NP_001341825.1:p.Thr2585Ser
NM_001354897.2:c.7729A>T	NP_001341826.1:p.Thr2577Ser
NM_001354898.2:c.7624A>T	NP_001341827.1:p.Thr2542Ser
NM_001354899.2:c.7615A>T	NP_001341828.1:p.Thr2539Ser
NM_001354900.2:c.7576A>T	NP_001341829.1:p.Thr2526Ser
NM_001354901.2:c.7522A>T	NP_001341830.1:p.Thr2508Ser
NM_001354902.2:c.7426A>T	NP_001341831.1:p.Thr2476Ser
NM_001354903.2:c.7396A>T	NP_001341832.1:p.Thr2466Ser
NM_001354904.2:c.7321A>T	NP_001341833.1:p.Thr2441Ser
NM_001354905.2:c.7219A>T	NP_001341834.1:p.Thr2407Ser
NM_001354906.2:c.6850A>T	NP_001341835.1:p.Thr2284Ser