Canonical Allele Identifier: CA16034200

Gene: APC

Linked Data

• dbSNP Id: rs2149951738
• MyVariant Identifiers: chr5:g.112177173T>A (hg19) ; chr5:g.112841476T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112841476T>A , CM000667.2:g.112841476T>A	GRCh38
NC_000005.9:g.112177173T>A , CM000667.1:g.112177173T>A	GRCh37
NC_000005.8:g.112205072T>A	NCBI36
NG_008481.4:g.153956T>A , LRG_130:g.153956T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.5936T>A	ENSP00000473355.2:p.Val1979Asp
ENST00000505350.2:c.*5888T>A	ENSP00000481752.1:n.*5888T>A
ENST00000507379.6:c.5828T>A	ENSP00000423224.2:p.Val1943Asp
ENST00000509732.6:c.5882T>A	ENSP00000426541.2:p.Val1961Asp
ENST00000512211.7:c.5882T>A	ENSP00000423828.3:p.Val1961Asp
ENST00000257430.9:c.5882T>A MANE Select	ENSP00000257430.4:p.Val1961Asp
ENST00000257430.8:c.5882T>A	ENSP00000257430.4:p.Val1961Asp
ENST00000508376.6:c.5882T>A	ENSP00000427089.2:p.Val1961Asp
ENST00000508624.5:c.*5204T>A	ENSP00000424265.1:n.*5204T>A
ENST00000520401.1:c.230+12504T>A
NM_000038.5:c.5882T>A	NP_000029.2:p.Val1961Asp
NM_001127510.2:c.5882T>A	NP_001120982.1:p.Val1961Asp
NM_001127511.2:c.5828T>A	NP_001120983.2:p.Val1943Asp
NM_001354895.1:c.5882T>A	NP_001341824.1:p.Val1961Asp
NM_001354896.1:c.5936T>A	NP_001341825.1:p.Val1979Asp
NM_001354897.1:c.5912T>A	NP_001341826.1:p.Val1971Asp
NM_001354898.1:c.5807T>A	NP_001341827.1:p.Val1936Asp
NM_001354899.1:c.5798T>A	NP_001341828.1:p.Val1933Asp
NM_001354900.1:c.5759T>A	NP_001341829.1:p.Val1920Asp
NM_001354901.1:c.5705T>A	NP_001341830.1:p.Val1902Asp
NM_001354902.1:c.5609T>A	NP_001341831.1:p.Val1870Asp
NM_001354903.1:c.5579T>A	NP_001341832.1:p.Val1860Asp
NM_001354904.1:c.5504T>A	NP_001341833.1:p.Val1835Asp
NM_001354905.1:c.5402T>A	NP_001341834.1:p.Val1801Asp
NM_001354906.1:c.5033T>A	NP_001341835.1:p.Val1678Asp
NM_000038.6:c.5882T>A MANE Select	NP_000029.2:p.Val1961Asp
NM_001127510.3:c.5882T>A	NP_001120982.1:p.Val1961Asp
NM_001127511.3:c.5828T>A	NP_001120983.2:p.Val1943Asp
NM_001354895.2:c.5882T>A	NP_001341824.1:p.Val1961Asp
NM_001354896.2:c.5936T>A	NP_001341825.1:p.Val1979Asp
NM_001354897.2:c.5912T>A	NP_001341826.1:p.Val1971Asp
NM_001354898.2:c.5807T>A	NP_001341827.1:p.Val1936Asp
NM_001354899.2:c.5798T>A	NP_001341828.1:p.Val1933Asp
NM_001354900.2:c.5759T>A	NP_001341829.1:p.Val1920Asp
NM_001354901.2:c.5705T>A	NP_001341830.1:p.Val1902Asp
NM_001354902.2:c.5609T>A	NP_001341831.1:p.Val1870Asp
NM_001354903.2:c.5579T>A	NP_001341832.1:p.Val1860Asp
NM_001354904.2:c.5504T>A	NP_001341833.1:p.Val1835Asp
NM_001354905.2:c.5402T>A	NP_001341834.1:p.Val1801Asp
NM_001354906.2:c.5033T>A	NP_001341835.1:p.Val1678Asp