Canonical Allele Identifier: CA16026174

Gene: APC

Linked Data

• ClinVar Variation Id: 2746817
• ClinVar RCV Id: RCV003536583
• dbSNP Id: rs2149863345
• MyVariant Identifiers: chr5:g.112173501A>T (hg19) ; chr5:g.112837804A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112837804A>T , CM000667.2:g.112837804A>T	GRCh38
NC_000005.9:g.112173501A>T , CM000667.1:g.112173501A>T	GRCh37
NC_000005.8:g.112201400A>T	NCBI36
NG_008481.4:g.150284A>T , LRG_130:g.150284A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1875A>T	ENSP00000484935.2:n.1875A>T
ENST00000504915.3:c.2264A>T	ENSP00000473355.2:p.Tyr755Phe
ENST00000505350.2:c.*2216A>T	ENSP00000481752.1:n.*2216A>T
ENST00000507379.6:c.2156A>T	ENSP00000423224.2:p.Tyr719Phe
ENST00000509732.6:c.2210A>T	ENSP00000426541.2:p.Tyr737Phe
ENST00000512211.7:c.2210A>T	ENSP00000423828.3:p.Tyr737Phe
ENST00000257430.9:c.2210A>T MANE Select	ENSP00000257430.4:p.Tyr737Phe
ENST00000257430.8:c.2210A>T	ENSP00000257430.4:p.Tyr737Phe
ENST00000502371.2:c.563A>T
ENST00000507379.5:c.2156A>T	ENSP00000423224.1:p.Tyr719Phe
ENST00000508376.6:c.2210A>T	ENSP00000427089.2:p.Tyr737Phe
ENST00000508624.5:c.*1532A>T	ENSP00000424265.1:n.*1532A>T
ENST00000512211.6:c.2210A>T	ENSP00000423828.2:p.Tyr737Phe
ENST00000520401.1:c.230+8832A>T
NM_000038.5:c.2210A>T	NP_000029.2:p.Tyr737Phe
NM_001127510.2:c.2210A>T	NP_001120982.1:p.Tyr737Phe
NM_001127511.2:c.2156A>T	NP_001120983.2:p.Tyr719Phe
NM_001354895.1:c.2210A>T	NP_001341824.1:p.Tyr737Phe
NM_001354896.1:c.2264A>T	NP_001341825.1:p.Tyr755Phe
NM_001354897.1:c.2240A>T	NP_001341826.1:p.Tyr747Phe
NM_001354898.1:c.2135A>T	NP_001341827.1:p.Tyr712Phe
NM_001354899.1:c.2126A>T	NP_001341828.1:p.Tyr709Phe
NM_001354900.1:c.2087A>T	NP_001341829.1:p.Tyr696Phe
NM_001354901.1:c.2033A>T	NP_001341830.1:p.Tyr678Phe
NM_001354902.1:c.1937A>T	NP_001341831.1:p.Tyr646Phe
NM_001354903.1:c.1907A>T	NP_001341832.1:p.Tyr636Phe
NM_001354904.1:c.1832A>T	NP_001341833.1:p.Tyr611Phe
NM_001354905.1:c.1730A>T	NP_001341834.1:p.Tyr577Phe
NM_001354906.1:c.1361A>T	NP_001341835.1:p.Tyr454Phe
NM_000038.6:c.2210A>T MANE Select	NP_000029.2:p.Tyr737Phe
NM_001127510.3:c.2210A>T	NP_001120982.1:p.Tyr737Phe
NM_001127511.3:c.2156A>T	NP_001120983.2:p.Tyr719Phe
NM_001354895.2:c.2210A>T	NP_001341824.1:p.Tyr737Phe
NM_001354896.2:c.2264A>T	NP_001341825.1:p.Tyr755Phe
NM_001354897.2:c.2240A>T	NP_001341826.1:p.Tyr747Phe
NM_001354898.2:c.2135A>T	NP_001341827.1:p.Tyr712Phe
NM_001354899.2:c.2126A>T	NP_001341828.1:p.Tyr709Phe
NM_001354900.2:c.2087A>T	NP_001341829.1:p.Tyr696Phe
NM_001354901.2:c.2033A>T	NP_001341830.1:p.Tyr678Phe
NM_001354902.2:c.1937A>T	NP_001341831.1:p.Tyr646Phe
NM_001354903.2:c.1907A>T	NP_001341832.1:p.Tyr636Phe
NM_001354904.2:c.1832A>T	NP_001341833.1:p.Tyr611Phe
NM_001354905.2:c.1730A>T	NP_001341834.1:p.Tyr577Phe
NM_001354906.2:c.1361A>T	NP_001341835.1:p.Tyr454Phe