Canonical Allele Identifier: CA16037917

Gene: APC

Linked Data

• ClinVar Variation Id: 1488918
• ClinVar RCV Id: RCV003745503
• dbSNP Id: rs2149991036
• MyVariant Identifiers: chr5:g.112178927A>T (hg19) ; chr5:g.112843230A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843230A>T , CM000667.2:g.112843230A>T	GRCh38
NC_000005.9:g.112178927A>T , CM000667.1:g.112178927A>T	GRCh37
NC_000005.8:g.112206826A>T	NCBI36
NG_008481.4:g.155710A>T , LRG_130:g.155710A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7690A>T	ENSP00000473355.2:p.Thr2564Ser
ENST00000505350.2:c.*7642A>T	ENSP00000481752.1:n.*7642A>T
ENST00000507379.6:c.7582A>T	ENSP00000423224.2:p.Thr2528Ser
ENST00000509732.6:c.7636A>T	ENSP00000426541.2:p.Thr2546Ser
ENST00000512211.7:c.7636A>T	ENSP00000423828.3:p.Thr2546Ser
ENST00000257430.9:c.7636A>T MANE Select	ENSP00000257430.4:p.Thr2546Ser
ENST00000257430.8:c.7636A>T	ENSP00000257430.4:p.Thr2546Ser
ENST00000508376.6:c.7636A>T	ENSP00000427089.2:p.Thr2546Ser
ENST00000520401.1:c.231-13419A>T
NM_000038.5:c.7636A>T	NP_000029.2:p.Thr2546Ser
NM_001127510.2:c.7636A>T	NP_001120982.1:p.Thr2546Ser
NM_001127511.2:c.7582A>T	NP_001120983.2:p.Thr2528Ser
NM_001354895.1:c.7636A>T	NP_001341824.1:p.Thr2546Ser
NM_001354896.1:c.7690A>T	NP_001341825.1:p.Thr2564Ser
NM_001354897.1:c.7666A>T	NP_001341826.1:p.Thr2556Ser
NM_001354898.1:c.7561A>T	NP_001341827.1:p.Thr2521Ser
NM_001354899.1:c.7552A>T	NP_001341828.1:p.Thr2518Ser
NM_001354900.1:c.7513A>T	NP_001341829.1:p.Thr2505Ser
NM_001354901.1:c.7459A>T	NP_001341830.1:p.Thr2487Ser
NM_001354902.1:c.7363A>T	NP_001341831.1:p.Thr2455Ser
NM_001354903.1:c.7333A>T	NP_001341832.1:p.Thr2445Ser
NM_001354904.1:c.7258A>T	NP_001341833.1:p.Thr2420Ser
NM_001354905.1:c.7156A>T	NP_001341834.1:p.Thr2386Ser
NM_001354906.1:c.6787A>T	NP_001341835.1:p.Thr2263Ser
NM_000038.6:c.7636A>T MANE Select	NP_000029.2:p.Thr2546Ser
NM_001127510.3:c.7636A>T	NP_001120982.1:p.Thr2546Ser
NM_001127511.3:c.7582A>T	NP_001120983.2:p.Thr2528Ser
NM_001354895.2:c.7636A>T	NP_001341824.1:p.Thr2546Ser
NM_001354896.2:c.7690A>T	NP_001341825.1:p.Thr2564Ser
NM_001354897.2:c.7666A>T	NP_001341826.1:p.Thr2556Ser
NM_001354898.2:c.7561A>T	NP_001341827.1:p.Thr2521Ser
NM_001354899.2:c.7552A>T	NP_001341828.1:p.Thr2518Ser
NM_001354900.2:c.7513A>T	NP_001341829.1:p.Thr2505Ser
NM_001354901.2:c.7459A>T	NP_001341830.1:p.Thr2487Ser
NM_001354902.2:c.7363A>T	NP_001341831.1:p.Thr2455Ser
NM_001354903.2:c.7333A>T	NP_001341832.1:p.Thr2445Ser
NM_001354904.2:c.7258A>T	NP_001341833.1:p.Thr2420Ser
NM_001354905.2:c.7156A>T	NP_001341834.1:p.Thr2386Ser
NM_001354906.2:c.6787A>T	NP_001341835.1:p.Thr2263Ser