Canonical Allele Identifier: CA16024331

Gene: APC

Linked Data

• COSMIC: COSM235650
• MyVariant Identifiers: chr5:g.112157661G>T (hg19) ; chr5:g.112821964G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112821964G>T , CM000667.2:g.112821964G>T	GRCh38
NC_000005.9:g.112157661G>T , CM000667.1:g.112157661G>T	GRCh37
NC_000005.8:g.112185560G>T	NCBI36
NG_008481.4:g.134444G>T , LRG_130:g.134444G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1381G>T	ENSP00000484935.2:p.Glu461Ter
ENST00000504915.3:c.1381G>T	ENSP00000473355.2:p.Glu461Ter
ENST00000505084.2:n.1437G>T
ENST00000505350.2:c.*1387G>T	ENSP00000481752.1:n.*1387G>T
ENST00000507379.6:c.1327G>T	ENSP00000423224.2:p.Glu443Ter
ENST00000509732.6:c.1381G>T	ENSP00000426541.2:p.Glu461Ter
ENST00000512211.7:c.1381G>T	ENSP00000423828.3:p.Glu461Ter
ENST00000257430.9:c.1381G>T MANE Select	ENSP00000257430.4:p.Glu461Ter
ENST00000257430.8:c.1381G>T	ENSP00000257430.4:p.Glu461Ter
ENST00000502371.2:c.69G>T
ENST00000504915.2:c.16G>T	ENSP00000473355.1:p.Glu6Ter
ENST00000507379.5:c.1327G>T	ENSP00000423224.1:p.Glu443Ter
ENST00000508376.6:c.1381G>T	ENSP00000427089.2:p.Glu461Ter
ENST00000508624.5:c.*703G>T	ENSP00000424265.1:n.*703G>T
ENST00000512211.6:c.1381G>T	ENSP00000423828.2:p.Glu461Ter
NM_000038.5:c.1381G>T	NP_000029.2:p.Glu461Ter
NM_001127510.2:c.1381G>T	NP_001120982.1:p.Glu461Ter
NM_001127511.2:c.1327G>T	NP_001120983.2:p.Glu443Ter
NM_001354895.1:c.1381G>T	NP_001341824.1:p.Glu461Ter
NM_001354896.1:c.1381G>T	NP_001341825.1:p.Glu461Ter
NM_001354897.1:c.1411G>T	NP_001341826.1:p.Glu471Ter
NM_001354898.1:c.1306G>T	NP_001341827.1:p.Glu436Ter
NM_001354899.1:c.1297G>T	NP_001341828.1:p.Glu433Ter
NM_001354900.1:c.1204G>T	NP_001341829.1:p.Glu402Ter
NM_001354901.1:c.1204G>T	NP_001341830.1:p.Glu402Ter
NM_001354902.1:c.1108G>T	NP_001341831.1:p.Glu370Ter
NM_001354903.1:c.1078G>T	NP_001341832.1:p.Glu360Ter
NM_001354904.1:c.1003G>T	NP_001341833.1:p.Glu335Ter
NM_001354905.1:c.901G>T	NP_001341834.1:p.Glu301Ter
NM_001354906.1:c.532G>T	NP_001341835.1:p.Glu178Ter
NM_000038.6:c.1381G>T MANE Select	NP_000029.2:p.Glu461Ter
NM_001127510.3:c.1381G>T	NP_001120982.1:p.Glu461Ter
NM_001127511.3:c.1327G>T	NP_001120983.2:p.Glu443Ter
NM_001354895.2:c.1381G>T	NP_001341824.1:p.Glu461Ter
NM_001354896.2:c.1381G>T	NP_001341825.1:p.Glu461Ter
NM_001354897.2:c.1411G>T	NP_001341826.1:p.Glu471Ter
NM_001354898.2:c.1306G>T	NP_001341827.1:p.Glu436Ter
NM_001354899.2:c.1297G>T	NP_001341828.1:p.Glu433Ter
NM_001354900.2:c.1204G>T	NP_001341829.1:p.Glu402Ter
NM_001354901.2:c.1204G>T	NP_001341830.1:p.Glu402Ter
NM_001354902.2:c.1108G>T	NP_001341831.1:p.Glu370Ter
NM_001354903.2:c.1078G>T	NP_001341832.1:p.Glu360Ter
NM_001354904.2:c.1003G>T	NP_001341833.1:p.Glu335Ter
NM_001354905.2:c.901G>T	NP_001341834.1:p.Glu301Ter
NM_001354906.2:c.532G>T	NP_001341835.1:p.Glu178Ter