Canonical Allele Identifier: CA16038627

Gene: APC

Linked Data

• ClinVar Variation Id: 2452710
• ClinVar RCV Id: RCV003177484
• dbSNP Id: rs2149997064
• MyVariant Identifiers: chr5:g.112179255A>T (hg19) ; chr5:g.112843558A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843558A>T , CM000667.2:g.112843558A>T	GRCh38
NC_000005.9:g.112179255A>T , CM000667.1:g.112179255A>T	GRCh37
NC_000005.8:g.112207154A>T	NCBI36
NG_008481.4:g.156038A>T , LRG_130:g.156038A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8018A>T	ENSP00000473355.2:p.Glu2673Val
ENST00000505350.2:c.*7970A>T	ENSP00000481752.1:n.*7970A>T
ENST00000507379.6:c.7910A>T	ENSP00000423224.2:p.Glu2637Val
ENST00000509732.6:c.7964A>T	ENSP00000426541.2:p.Glu2655Val
ENST00000512211.7:c.7964A>T	ENSP00000423828.3:p.Glu2655Val
ENST00000257430.9:c.7964A>T MANE Select	ENSP00000257430.4:p.Glu2655Val
ENST00000257430.8:c.7964A>T	ENSP00000257430.4:p.Glu2655Val
ENST00000508376.6:c.7964A>T	ENSP00000427089.2:p.Glu2655Val
ENST00000520401.1:c.231-13091A>T
NM_000038.5:c.7964A>T	NP_000029.2:p.Glu2655Val
NM_001127510.2:c.7964A>T	NP_001120982.1:p.Glu2655Val
NM_001127511.2:c.7910A>T	NP_001120983.2:p.Glu2637Val
NM_001354895.1:c.7964A>T	NP_001341824.1:p.Glu2655Val
NM_001354896.1:c.8018A>T	NP_001341825.1:p.Glu2673Val
NM_001354897.1:c.7994A>T	NP_001341826.1:p.Glu2665Val
NM_001354898.1:c.7889A>T	NP_001341827.1:p.Glu2630Val
NM_001354899.1:c.7880A>T	NP_001341828.1:p.Glu2627Val
NM_001354900.1:c.7841A>T	NP_001341829.1:p.Glu2614Val
NM_001354901.1:c.7787A>T	NP_001341830.1:p.Glu2596Val
NM_001354902.1:c.7691A>T	NP_001341831.1:p.Glu2564Val
NM_001354903.1:c.7661A>T	NP_001341832.1:p.Glu2554Val
NM_001354904.1:c.7586A>T	NP_001341833.1:p.Glu2529Val
NM_001354905.1:c.7484A>T	NP_001341834.1:p.Glu2495Val
NM_001354906.1:c.7115A>T	NP_001341835.1:p.Glu2372Val
NM_000038.6:c.7964A>T MANE Select	NP_000029.2:p.Glu2655Val
NM_001127510.3:c.7964A>T	NP_001120982.1:p.Glu2655Val
NM_001127511.3:c.7910A>T	NP_001120983.2:p.Glu2637Val
NM_001354895.2:c.7964A>T	NP_001341824.1:p.Glu2655Val
NM_001354896.2:c.8018A>T	NP_001341825.1:p.Glu2673Val
NM_001354897.2:c.7994A>T	NP_001341826.1:p.Glu2665Val
NM_001354898.2:c.7889A>T	NP_001341827.1:p.Glu2630Val
NM_001354899.2:c.7880A>T	NP_001341828.1:p.Glu2627Val
NM_001354900.2:c.7841A>T	NP_001341829.1:p.Glu2614Val
NM_001354901.2:c.7787A>T	NP_001341830.1:p.Glu2596Val
NM_001354902.2:c.7691A>T	NP_001341831.1:p.Glu2564Val
NM_001354903.2:c.7661A>T	NP_001341832.1:p.Glu2554Val
NM_001354904.2:c.7586A>T	NP_001341833.1:p.Glu2529Val
NM_001354905.2:c.7484A>T	NP_001341834.1:p.Glu2495Val
NM_001354906.2:c.7115A>T	NP_001341835.1:p.Glu2372Val