Canonical Allele Identifier: CA16032129

Gene: APC

Linked Data

• dbSNP Id: rs2149927688
• MyVariant Identifiers: chr5:g.112176221G>T (hg19) ; chr5:g.112840524G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840524G>T , CM000667.2:g.112840524G>T	GRCh38
NC_000005.9:g.112176221G>T , CM000667.1:g.112176221G>T	GRCh37
NC_000005.8:g.112204120G>T	NCBI36
NG_008481.4:g.153004G>T , LRG_130:g.153004G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4984G>T	ENSP00000473355.2:p.Val1662Phe
ENST00000505350.2:c.*4936G>T	ENSP00000481752.1:n.*4936G>T
ENST00000507379.6:c.4876G>T	ENSP00000423224.2:p.Val1626Phe
ENST00000509732.6:c.4930G>T	ENSP00000426541.2:p.Val1644Phe
ENST00000512211.7:c.4930G>T	ENSP00000423828.3:p.Val1644Phe
ENST00000257430.9:c.4930G>T MANE Select	ENSP00000257430.4:p.Val1644Phe
ENST00000257430.8:c.4930G>T	ENSP00000257430.4:p.Val1644Phe
ENST00000508376.6:c.4930G>T	ENSP00000427089.2:p.Val1644Phe
ENST00000508624.5:c.*4252G>T	ENSP00000424265.1:n.*4252G>T
ENST00000520401.1:c.230+11552G>T
NM_000038.5:c.4930G>T	NP_000029.2:p.Val1644Phe
NM_001127510.2:c.4930G>T	NP_001120982.1:p.Val1644Phe
NM_001127511.2:c.4876G>T	NP_001120983.2:p.Val1626Phe
NM_001354895.1:c.4930G>T	NP_001341824.1:p.Val1644Phe
NM_001354896.1:c.4984G>T	NP_001341825.1:p.Val1662Phe
NM_001354897.1:c.4960G>T	NP_001341826.1:p.Val1654Phe
NM_001354898.1:c.4855G>T	NP_001341827.1:p.Val1619Phe
NM_001354899.1:c.4846G>T	NP_001341828.1:p.Val1616Phe
NM_001354900.1:c.4807G>T	NP_001341829.1:p.Val1603Phe
NM_001354901.1:c.4753G>T	NP_001341830.1:p.Val1585Phe
NM_001354902.1:c.4657G>T	NP_001341831.1:p.Val1553Phe
NM_001354903.1:c.4627G>T	NP_001341832.1:p.Val1543Phe
NM_001354904.1:c.4552G>T	NP_001341833.1:p.Val1518Phe
NM_001354905.1:c.4450G>T	NP_001341834.1:p.Val1484Phe
NM_001354906.1:c.4081G>T	NP_001341835.1:p.Val1361Phe
NM_000038.6:c.4930G>T MANE Select	NP_000029.2:p.Val1644Phe
NM_001127510.3:c.4930G>T	NP_001120982.1:p.Val1644Phe
NM_001127511.3:c.4876G>T	NP_001120983.2:p.Val1626Phe
NM_001354895.2:c.4930G>T	NP_001341824.1:p.Val1644Phe
NM_001354896.2:c.4984G>T	NP_001341825.1:p.Val1662Phe
NM_001354897.2:c.4960G>T	NP_001341826.1:p.Val1654Phe
NM_001354898.2:c.4855G>T	NP_001341827.1:p.Val1619Phe
NM_001354899.2:c.4846G>T	NP_001341828.1:p.Val1616Phe
NM_001354900.2:c.4807G>T	NP_001341829.1:p.Val1603Phe
NM_001354901.2:c.4753G>T	NP_001341830.1:p.Val1585Phe
NM_001354902.2:c.4657G>T	NP_001341831.1:p.Val1553Phe
NM_001354903.2:c.4627G>T	NP_001341832.1:p.Val1543Phe
NM_001354904.2:c.4552G>T	NP_001341833.1:p.Val1518Phe
NM_001354905.2:c.4450G>T	NP_001341834.1:p.Val1484Phe
NM_001354906.2:c.4081G>T	NP_001341835.1:p.Val1361Phe