Canonical Allele Identifier: CA16032068

Gene: APC

Linked Data

• dbSNP Id: rs765215625
• MyVariant Identifiers: chr5:g.112176189C>G (hg19) ; chr5:g.112840492C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840492C>G , CM000667.2:g.112840492C>G	GRCh38
NC_000005.9:g.112176189C>G , CM000667.1:g.112176189C>G	GRCh37
NC_000005.8:g.112204088C>G	NCBI36
NG_008481.4:g.152972C>G , LRG_130:g.152972C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4952C>G	ENSP00000473355.2:p.Thr1651Arg
ENST00000505350.2:c.*4904C>G	ENSP00000481752.1:n.*4904C>G
ENST00000507379.6:c.4844C>G	ENSP00000423224.2:p.Thr1615Arg
ENST00000509732.6:c.4898C>G	ENSP00000426541.2:p.Thr1633Arg
ENST00000512211.7:c.4898C>G	ENSP00000423828.3:p.Thr1633Arg
ENST00000257430.9:c.4898C>G MANE Select	ENSP00000257430.4:p.Thr1633Arg
ENST00000257430.8:c.4898C>G	ENSP00000257430.4:p.Thr1633Arg
ENST00000508376.6:c.4898C>G	ENSP00000427089.2:p.Thr1633Arg
ENST00000508624.5:c.*4220C>G	ENSP00000424265.1:n.*4220C>G
ENST00000520401.1:c.230+11520C>G
NM_000038.5:c.4898C>G	NP_000029.2:p.Thr1633Arg
NM_001127510.2:c.4898C>G	NP_001120982.1:p.Thr1633Arg
NM_001127511.2:c.4844C>G	NP_001120983.2:p.Thr1615Arg
NM_001354895.1:c.4898C>G	NP_001341824.1:p.Thr1633Arg
NM_001354896.1:c.4952C>G	NP_001341825.1:p.Thr1651Arg
NM_001354897.1:c.4928C>G	NP_001341826.1:p.Thr1643Arg
NM_001354898.1:c.4823C>G	NP_001341827.1:p.Thr1608Arg
NM_001354899.1:c.4814C>G	NP_001341828.1:p.Thr1605Arg
NM_001354900.1:c.4775C>G	NP_001341829.1:p.Thr1592Arg
NM_001354901.1:c.4721C>G	NP_001341830.1:p.Thr1574Arg
NM_001354902.1:c.4625C>G	NP_001341831.1:p.Thr1542Arg
NM_001354903.1:c.4595C>G	NP_001341832.1:p.Thr1532Arg
NM_001354904.1:c.4520C>G	NP_001341833.1:p.Thr1507Arg
NM_001354905.1:c.4418C>G	NP_001341834.1:p.Thr1473Arg
NM_001354906.1:c.4049C>G	NP_001341835.1:p.Thr1350Arg
NM_000038.6:c.4898C>G MANE Select	NP_000029.2:p.Thr1633Arg
NM_001127510.3:c.4898C>G	NP_001120982.1:p.Thr1633Arg
NM_001127511.3:c.4844C>G	NP_001120983.2:p.Thr1615Arg
NM_001354895.2:c.4898C>G	NP_001341824.1:p.Thr1633Arg
NM_001354896.2:c.4952C>G	NP_001341825.1:p.Thr1651Arg
NM_001354897.2:c.4928C>G	NP_001341826.1:p.Thr1643Arg
NM_001354898.2:c.4823C>G	NP_001341827.1:p.Thr1608Arg
NM_001354899.2:c.4814C>G	NP_001341828.1:p.Thr1605Arg
NM_001354900.2:c.4775C>G	NP_001341829.1:p.Thr1592Arg
NM_001354901.2:c.4721C>G	NP_001341830.1:p.Thr1574Arg
NM_001354902.2:c.4625C>G	NP_001341831.1:p.Thr1542Arg
NM_001354903.2:c.4595C>G	NP_001341832.1:p.Thr1532Arg
NM_001354904.2:c.4520C>G	NP_001341833.1:p.Thr1507Arg
NM_001354905.2:c.4418C>G	NP_001341834.1:p.Thr1473Arg
NM_001354906.2:c.4049C>G	NP_001341835.1:p.Thr1350Arg