Canonical Allele Identifier: CA446209599

Gene: APC

Linked Data

• gnomAD v4: 5-112840721-C-T
• MyVariant Identifiers: chr5:g.112176418C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840721C>T , CM000667.2:g.112840721C>T	GRCh38
NC_000005.9:g.112176418C>T , CM000667.1:g.112176418C>T	GRCh37
NC_000005.8:g.112204317C>T	NCBI36
NG_008481.4:g.153201C>T , LRG_130:g.153201C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5181C>T	ENSP00000473355.2:p.Thr1727=
ENST00000505350.2:c.*5133C>T	ENSP00000481752.1:n.*5133C>T
ENST00000507379.6:c.5073C>T	ENSP00000423224.2:p.Thr1691=
ENST00000509732.6:c.5127C>T	ENSP00000426541.2:p.Thr1709=
ENST00000512211.7:c.5127C>T	ENSP00000423828.3:p.Thr1709=
ENST00000257430.9:c.5127C>T MANE Select	ENSP00000257430.4:p.Thr1709=
ENST00000257430.8:c.5127C>T	ENSP00000257430.4:p.Thr1709=
ENST00000508376.6:c.5127C>T	ENSP00000427089.2:p.Thr1709=
ENST00000508624.5:c.*4449C>T	ENSP00000424265.1:n.*4449C>T
ENST00000520401.1:c.230+11749C>T
NM_000038.5:c.5127C>T	NP_000029.2:p.Thr1709=
NM_001127510.2:c.5127C>T	NP_001120982.1:p.Thr1709=
NM_001127511.2:c.5073C>T	NP_001120983.2:p.Thr1691=
NM_001354895.1:c.5127C>T	NP_001341824.1:p.Thr1709=
NM_001354896.1:c.5181C>T	NP_001341825.1:p.Thr1727=
NM_001354897.1:c.5157C>T	NP_001341826.1:p.Thr1719=
NM_001354898.1:c.5052C>T	NP_001341827.1:p.Thr1684=
NM_001354899.1:c.5043C>T	NP_001341828.1:p.Thr1681=
NM_001354900.1:c.5004C>T	NP_001341829.1:p.Thr1668=
NM_001354901.1:c.4950C>T	NP_001341830.1:p.Thr1650=
NM_001354902.1:c.4854C>T	NP_001341831.1:p.Thr1618=
NM_001354903.1:c.4824C>T	NP_001341832.1:p.Thr1608=
NM_001354904.1:c.4749C>T	NP_001341833.1:p.Thr1583=
NM_001354905.1:c.4647C>T	NP_001341834.1:p.Thr1549=
NM_001354906.1:c.4278C>T	NP_001341835.1:p.Thr1426=
NM_000038.6:c.5127C>T MANE Select	NP_000029.2:p.Thr1709=
NM_001127510.3:c.5127C>T	NP_001120982.1:p.Thr1709=
NM_001127511.3:c.5073C>T	NP_001120983.2:p.Thr1691=
NM_001354895.2:c.5127C>T	NP_001341824.1:p.Thr1709=
NM_001354896.2:c.5181C>T	NP_001341825.1:p.Thr1727=
NM_001354897.2:c.5157C>T	NP_001341826.1:p.Thr1719=
NM_001354898.2:c.5052C>T	NP_001341827.1:p.Thr1684=
NM_001354899.2:c.5043C>T	NP_001341828.1:p.Thr1681=
NM_001354900.2:c.5004C>T	NP_001341829.1:p.Thr1668=
NM_001354901.2:c.4950C>T	NP_001341830.1:p.Thr1650=
NM_001354902.2:c.4854C>T	NP_001341831.1:p.Thr1618=
NM_001354903.2:c.4824C>T	NP_001341832.1:p.Thr1608=
NM_001354904.2:c.4749C>T	NP_001341833.1:p.Thr1583=
NM_001354905.2:c.4647C>T	NP_001341834.1:p.Thr1549=
NM_001354906.2:c.4278C>T	NP_001341835.1:p.Thr1426=