Canonical Allele Identifier: CA446210924

Gene: APC

Linked Data

• ClinVar Variation Id: 1760939
• ClinVar RCV Id: RCV002412252
• dbSNP Id: rs775126492
• MyVariant Identifiers: chr5:g.112179160A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843463A>T , CM000667.2:g.112843463A>T	GRCh38
NC_000005.9:g.112179160A>T , CM000667.1:g.112179160A>T	GRCh37
NC_000005.8:g.112207059A>T	NCBI36
NG_008481.4:g.155943A>T , LRG_130:g.155943A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7923A>T	ENSP00000473355.2:p.Thr2641=
ENST00000505350.2:c.*7875A>T	ENSP00000481752.1:n.*7875A>T
ENST00000507379.6:c.7815A>T	ENSP00000423224.2:p.Thr2605=
ENST00000509732.6:c.7869A>T	ENSP00000426541.2:p.Thr2623=
ENST00000512211.7:c.7869A>T	ENSP00000423828.3:p.Thr2623=
ENST00000257430.9:c.7869A>T MANE Select	ENSP00000257430.4:p.Thr2623=
ENST00000257430.8:c.7869A>T	ENSP00000257430.4:p.Thr2623=
ENST00000508376.6:c.7869A>T	ENSP00000427089.2:p.Thr2623=
ENST00000520401.1:c.231-13186A>T
NM_000038.5:c.7869A>T	NP_000029.2:p.Thr2623=
NM_001127510.2:c.7869A>T	NP_001120982.1:p.Thr2623=
NM_001127511.2:c.7815A>T	NP_001120983.2:p.Thr2605=
NM_001354895.1:c.7869A>T	NP_001341824.1:p.Thr2623=
NM_001354896.1:c.7923A>T	NP_001341825.1:p.Thr2641=
NM_001354897.1:c.7899A>T	NP_001341826.1:p.Thr2633=
NM_001354898.1:c.7794A>T	NP_001341827.1:p.Thr2598=
NM_001354899.1:c.7785A>T	NP_001341828.1:p.Thr2595=
NM_001354900.1:c.7746A>T	NP_001341829.1:p.Thr2582=
NM_001354901.1:c.7692A>T	NP_001341830.1:p.Thr2564=
NM_001354902.1:c.7596A>T	NP_001341831.1:p.Thr2532=
NM_001354903.1:c.7566A>T	NP_001341832.1:p.Thr2522=
NM_001354904.1:c.7491A>T	NP_001341833.1:p.Thr2497=
NM_001354905.1:c.7389A>T	NP_001341834.1:p.Thr2463=
NM_001354906.1:c.7020A>T	NP_001341835.1:p.Thr2340=
NM_000038.6:c.7869A>T MANE Select	NP_000029.2:p.Thr2623=
NM_001127510.3:c.7869A>T	NP_001120982.1:p.Thr2623=
NM_001127511.3:c.7815A>T	NP_001120983.2:p.Thr2605=
NM_001354895.2:c.7869A>T	NP_001341824.1:p.Thr2623=
NM_001354896.2:c.7923A>T	NP_001341825.1:p.Thr2641=
NM_001354897.2:c.7899A>T	NP_001341826.1:p.Thr2633=
NM_001354898.2:c.7794A>T	NP_001341827.1:p.Thr2598=
NM_001354899.2:c.7785A>T	NP_001341828.1:p.Thr2595=
NM_001354900.2:c.7746A>T	NP_001341829.1:p.Thr2582=
NM_001354901.2:c.7692A>T	NP_001341830.1:p.Thr2564=
NM_001354902.2:c.7596A>T	NP_001341831.1:p.Thr2532=
NM_001354903.2:c.7566A>T	NP_001341832.1:p.Thr2522=
NM_001354904.2:c.7491A>T	NP_001341833.1:p.Thr2497=
NM_001354905.2:c.7389A>T	NP_001341834.1:p.Thr2463=
NM_001354906.2:c.7020A>T	NP_001341835.1:p.Thr2340=