Canonical Allele Identifier: CA16033005

Gene: APC

Linked Data

• ClinVar Variation Id: 469995
• ClinVar RCV Id: RCV003337310 ; RCV003742730
• dbSNP Id: rs1554086653
• MyVariant Identifiers: chr5:g.112176632C>T (hg19) ; chr5:g.112840935C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840935C>T , CM000667.2:g.112840935C>T	GRCh38
NC_000005.9:g.112176632C>T , CM000667.1:g.112176632C>T	GRCh37
NC_000005.8:g.112204531C>T	NCBI36
NG_008481.4:g.153415C>T , LRG_130:g.153415C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5395C>T	ENSP00000473355.2:p.Gln1799Ter
ENST00000505350.2:c.*5347C>T	ENSP00000481752.1:n.*5347C>T
ENST00000507379.6:c.5287C>T	ENSP00000423224.2:p.Gln1763Ter
ENST00000509732.6:c.5341C>T	ENSP00000426541.2:p.Gln1781Ter
ENST00000512211.7:c.5341C>T	ENSP00000423828.3:p.Gln1781Ter
ENST00000257430.9:c.5341C>T MANE Select	ENSP00000257430.4:p.Gln1781Ter
ENST00000257430.8:c.5341C>T	ENSP00000257430.4:p.Gln1781Ter
ENST00000508376.6:c.5341C>T	ENSP00000427089.2:p.Gln1781Ter
ENST00000508624.5:c.*4663C>T	ENSP00000424265.1:n.*4663C>T
ENST00000520401.1:c.230+11963C>T
NM_000038.5:c.5341C>T	NP_000029.2:p.Gln1781Ter
NM_001127510.2:c.5341C>T	NP_001120982.1:p.Gln1781Ter
NM_001127511.2:c.5287C>T	NP_001120983.2:p.Gln1763Ter
NM_001354895.1:c.5341C>T	NP_001341824.1:p.Gln1781Ter
NM_001354896.1:c.5395C>T	NP_001341825.1:p.Gln1799Ter
NM_001354897.1:c.5371C>T	NP_001341826.1:p.Gln1791Ter
NM_001354898.1:c.5266C>T	NP_001341827.1:p.Gln1756Ter
NM_001354899.1:c.5257C>T	NP_001341828.1:p.Gln1753Ter
NM_001354900.1:c.5218C>T	NP_001341829.1:p.Gln1740Ter
NM_001354901.1:c.5164C>T	NP_001341830.1:p.Gln1722Ter
NM_001354902.1:c.5068C>T	NP_001341831.1:p.Gln1690Ter
NM_001354903.1:c.5038C>T	NP_001341832.1:p.Gln1680Ter
NM_001354904.1:c.4963C>T	NP_001341833.1:p.Gln1655Ter
NM_001354905.1:c.4861C>T	NP_001341834.1:p.Gln1621Ter
NM_001354906.1:c.4492C>T	NP_001341835.1:p.Gln1498Ter
NM_000038.6:c.5341C>T MANE Select	NP_000029.2:p.Gln1781Ter
NM_001127510.3:c.5341C>T	NP_001120982.1:p.Gln1781Ter
NM_001127511.3:c.5287C>T	NP_001120983.2:p.Gln1763Ter
NM_001354895.2:c.5341C>T	NP_001341824.1:p.Gln1781Ter
NM_001354896.2:c.5395C>T	NP_001341825.1:p.Gln1799Ter
NM_001354897.2:c.5371C>T	NP_001341826.1:p.Gln1791Ter
NM_001354898.2:c.5266C>T	NP_001341827.1:p.Gln1756Ter
NM_001354899.2:c.5257C>T	NP_001341828.1:p.Gln1753Ter
NM_001354900.2:c.5218C>T	NP_001341829.1:p.Gln1740Ter
NM_001354901.2:c.5164C>T	NP_001341830.1:p.Gln1722Ter
NM_001354902.2:c.5068C>T	NP_001341831.1:p.Gln1690Ter
NM_001354903.2:c.5038C>T	NP_001341832.1:p.Gln1680Ter
NM_001354904.2:c.4963C>T	NP_001341833.1:p.Gln1655Ter
NM_001354905.2:c.4861C>T	NP_001341834.1:p.Gln1621Ter
NM_001354906.2:c.4492C>T	NP_001341835.1:p.Gln1498Ter