Canonical Allele Identifier: CA279782

Gene: APC

Linked Data

• ClinVar Variation Id: 217918
• ClinVar RCV Id: RCV000202206 ; RCV002399752 ; RCV003743625
• dbSNP Id: rs863225307
• MyVariant Identifiers: chr5:g.112154774C>T (hg19) ; chr5:g.112819077C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112819077C>T , CM000667.2:g.112819077C>T	GRCh38
NC_000005.9:g.112154774C>T , CM000667.1:g.112154774C>T	GRCh37
NC_000005.8:g.112182673C>T	NCBI36
NG_008481.4:g.131557C>T , LRG_130:g.131557C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1045C>T	ENSP00000484935.2:p.Gln349Ter
ENST00000504915.3:c.1045C>T	ENSP00000473355.2:p.Gln349Ter
ENST00000505084.2:n.1101C>T
ENST00000505350.2:c.*1051C>T	ENSP00000481752.1:n.*1051C>T
ENST00000507379.6:c.991C>T	ENSP00000423224.2:p.Gln331Ter
ENST00000509732.6:c.1045C>T	ENSP00000426541.2:p.Gln349Ter
ENST00000512211.7:c.1045C>T	ENSP00000423828.3:p.Gln349Ter
ENST00000257430.9:c.1045C>T MANE Select	ENSP00000257430.4:p.Gln349Ter
ENST00000257430.8:c.1045C>T	ENSP00000257430.4:p.Gln349Ter
ENST00000507379.5:c.991C>T	ENSP00000423224.1:p.Gln331Ter
ENST00000508376.6:c.1045C>T	ENSP00000427089.2:p.Gln349Ter
ENST00000508624.5:c.*367C>T	ENSP00000424265.1:n.*367C>T
ENST00000512211.6:c.1045C>T	ENSP00000423828.2:p.Gln349Ter
NM_000038.5:c.1045C>T	NP_000029.2:p.Gln349Ter
NM_001127510.2:c.1045C>T	NP_001120982.1:p.Gln349Ter
NM_001127511.2:c.991C>T	NP_001120983.2:p.Gln331Ter
NM_001354895.1:c.1045C>T	NP_001341824.1:p.Gln349Ter
NM_001354896.1:c.1045C>T	NP_001341825.1:p.Gln349Ter
NM_001354897.1:c.1075C>T	NP_001341826.1:p.Gln359Ter
NM_001354898.1:c.970C>T	NP_001341827.1:p.Gln324Ter
NM_001354899.1:c.961C>T	NP_001341828.1:p.Gln321Ter
NM_001354900.1:c.868C>T	NP_001341829.1:p.Gln290Ter
NM_001354901.1:c.868C>T	NP_001341830.1:p.Gln290Ter
NM_001354902.1:c.964-192C>T	NP_001341831.1:n.964-192C>T
NM_001354903.1:c.934-192C>T	NP_001341832.1:n.934-192C>T
NM_001354904.1:c.859-192C>T	NP_001341833.1:n.859-192C>T
NM_001354905.1:c.757-192C>T	NP_001341834.1:n.757-192C>T
NM_001354906.1:c.196C>T	NP_001341835.1:p.Gln66Ter
NM_000038.6:c.1045C>T MANE Select	NP_000029.2:p.Gln349Ter
NM_001127510.3:c.1045C>T	NP_001120982.1:p.Gln349Ter
NM_001127511.3:c.991C>T	NP_001120983.2:p.Gln331Ter
NM_001354895.2:c.1045C>T	NP_001341824.1:p.Gln349Ter
NM_001354896.2:c.1045C>T	NP_001341825.1:p.Gln349Ter
NM_001354897.2:c.1075C>T	NP_001341826.1:p.Gln359Ter
NM_001354898.2:c.970C>T	NP_001341827.1:p.Gln324Ter
NM_001354899.2:c.961C>T	NP_001341828.1:p.Gln321Ter
NM_001354900.2:c.868C>T	NP_001341829.1:p.Gln290Ter
NM_001354901.2:c.868C>T	NP_001341830.1:p.Gln290Ter
NM_001354902.2:c.964-192C>T	NP_001341831.1:n.964-192C>T
NM_001354903.2:c.934-192C>T	NP_001341832.1:n.934-192C>T
NM_001354904.2:c.859-192C>T	NP_001341833.1:n.859-192C>T
NM_001354905.2:c.757-192C>T	NP_001341834.1:n.757-192C>T
NM_001354906.2:c.196C>T	NP_001341835.1:p.Gln66Ter