Canonical Allele Identifier: CA16032909

Gene: APC

Linked Data

• dbSNP Id: rs1580658487
• MyVariant Identifiers: chr5:g.112176587G>T (hg19) ; chr5:g.112840890G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840890G>T , CM000667.2:g.112840890G>T	GRCh38
NC_000005.9:g.112176587G>T , CM000667.1:g.112176587G>T	GRCh37
NC_000005.8:g.112204486G>T	NCBI36
NG_008481.4:g.153370G>T , LRG_130:g.153370G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.5350G>T	ENSP00000473355.2:p.Asp1784Tyr
ENST00000505350.2:c.*5302G>T	ENSP00000481752.1:n.*5302G>T
ENST00000507379.6:c.5242G>T	ENSP00000423224.2:p.Asp1748Tyr
ENST00000509732.6:c.5296G>T	ENSP00000426541.2:p.Asp1766Tyr
ENST00000512211.7:c.5296G>T	ENSP00000423828.3:p.Asp1766Tyr
ENST00000257430.9:c.5296G>T MANE Select	ENSP00000257430.4:p.Asp1766Tyr
ENST00000257430.8:c.5296G>T	ENSP00000257430.4:p.Asp1766Tyr
ENST00000508376.6:c.5296G>T	ENSP00000427089.2:p.Asp1766Tyr
ENST00000508624.5:c.*4618G>T	ENSP00000424265.1:n.*4618G>T
ENST00000520401.1:c.230+11918G>T
NM_000038.5:c.5296G>T	NP_000029.2:p.Asp1766Tyr
NM_001127510.2:c.5296G>T	NP_001120982.1:p.Asp1766Tyr
NM_001127511.2:c.5242G>T	NP_001120983.2:p.Asp1748Tyr
NM_001354895.1:c.5296G>T	NP_001341824.1:p.Asp1766Tyr
NM_001354896.1:c.5350G>T	NP_001341825.1:p.Asp1784Tyr
NM_001354897.1:c.5326G>T	NP_001341826.1:p.Asp1776Tyr
NM_001354898.1:c.5221G>T	NP_001341827.1:p.Asp1741Tyr
NM_001354899.1:c.5212G>T	NP_001341828.1:p.Asp1738Tyr
NM_001354900.1:c.5173G>T	NP_001341829.1:p.Asp1725Tyr
NM_001354901.1:c.5119G>T	NP_001341830.1:p.Asp1707Tyr
NM_001354902.1:c.5023G>T	NP_001341831.1:p.Asp1675Tyr
NM_001354903.1:c.4993G>T	NP_001341832.1:p.Asp1665Tyr
NM_001354904.1:c.4918G>T	NP_001341833.1:p.Asp1640Tyr
NM_001354905.1:c.4816G>T	NP_001341834.1:p.Asp1606Tyr
NM_001354906.1:c.4447G>T	NP_001341835.1:p.Asp1483Tyr
NM_000038.6:c.5296G>T MANE Select	NP_000029.2:p.Asp1766Tyr
NM_001127510.3:c.5296G>T	NP_001120982.1:p.Asp1766Tyr
NM_001127511.3:c.5242G>T	NP_001120983.2:p.Asp1748Tyr
NM_001354895.2:c.5296G>T	NP_001341824.1:p.Asp1766Tyr
NM_001354896.2:c.5350G>T	NP_001341825.1:p.Asp1784Tyr
NM_001354897.2:c.5326G>T	NP_001341826.1:p.Asp1776Tyr
NM_001354898.2:c.5221G>T	NP_001341827.1:p.Asp1741Tyr
NM_001354899.2:c.5212G>T	NP_001341828.1:p.Asp1738Tyr
NM_001354900.2:c.5173G>T	NP_001341829.1:p.Asp1725Tyr
NM_001354901.2:c.5119G>T	NP_001341830.1:p.Asp1707Tyr
NM_001354902.2:c.5023G>T	NP_001341831.1:p.Asp1675Tyr
NM_001354903.2:c.4993G>T	NP_001341832.1:p.Asp1665Tyr
NM_001354904.2:c.4918G>T	NP_001341833.1:p.Asp1640Tyr
NM_001354905.2:c.4816G>T	NP_001341834.1:p.Asp1606Tyr
NM_001354906.2:c.4447G>T	NP_001341835.1:p.Asp1483Tyr