Canonical Allele Identifier: CA16028167

Gene: APC

Linked Data

• dbSNP Id: rs1178716584
• gnomAD v4: 5-112838713-G-T
• MyVariant Identifiers: chr5:g.112174410G>T (hg19) ; chr5:g.112838713G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838713G>T , CM000667.2:g.112838713G>T	GRCh38
NC_000005.9:g.112174410G>T , CM000667.1:g.112174410G>T	GRCh37
NC_000005.8:g.112202309G>T	NCBI36
NG_008481.4:g.151193G>T , LRG_130:g.151193G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2784G>T	ENSP00000484935.2:n.2784G>T
ENST00000504915.3:c.3173G>T	ENSP00000473355.2:p.Arg1058Met
ENST00000505350.2:c.*3125G>T	ENSP00000481752.1:n.*3125G>T
ENST00000507379.6:c.3065G>T	ENSP00000423224.2:p.Arg1022Met
ENST00000509732.6:c.3119G>T	ENSP00000426541.2:p.Arg1040Met
ENST00000512211.7:c.3119G>T	ENSP00000423828.3:p.Arg1040Met
ENST00000257430.9:c.3119G>T MANE Select	ENSP00000257430.4:p.Arg1040Met
ENST00000257430.8:c.3119G>T	ENSP00000257430.4:p.Arg1040Met
ENST00000502371.2:c.1472G>T
ENST00000507379.5:c.3065G>T	ENSP00000423224.1:p.Arg1022Met
ENST00000508376.6:c.3119G>T	ENSP00000427089.2:p.Arg1040Met
ENST00000508624.5:c.*2441G>T	ENSP00000424265.1:n.*2441G>T
ENST00000512211.6:c.3119G>T	ENSP00000423828.2:p.Arg1040Met
ENST00000520401.1:c.230+9741G>T
NM_000038.5:c.3119G>T	NP_000029.2:p.Arg1040Met
NM_001127510.2:c.3119G>T	NP_001120982.1:p.Arg1040Met
NM_001127511.2:c.3065G>T	NP_001120983.2:p.Arg1022Met
NM_001354895.1:c.3119G>T	NP_001341824.1:p.Arg1040Met
NM_001354896.1:c.3173G>T	NP_001341825.1:p.Arg1058Met
NM_001354897.1:c.3149G>T	NP_001341826.1:p.Arg1050Met
NM_001354898.1:c.3044G>T	NP_001341827.1:p.Arg1015Met
NM_001354899.1:c.3035G>T	NP_001341828.1:p.Arg1012Met
NM_001354900.1:c.2996G>T	NP_001341829.1:p.Arg999Met
NM_001354901.1:c.2942G>T	NP_001341830.1:p.Arg981Met
NM_001354902.1:c.2846G>T	NP_001341831.1:p.Arg949Met
NM_001354903.1:c.2816G>T	NP_001341832.1:p.Arg939Met
NM_001354904.1:c.2741G>T	NP_001341833.1:p.Arg914Met
NM_001354905.1:c.2639G>T	NP_001341834.1:p.Arg880Met
NM_001354906.1:c.2270G>T	NP_001341835.1:p.Arg757Met
NM_000038.6:c.3119G>T MANE Select	NP_000029.2:p.Arg1040Met
NM_001127510.3:c.3119G>T	NP_001120982.1:p.Arg1040Met
NM_001127511.3:c.3065G>T	NP_001120983.2:p.Arg1022Met
NM_001354895.2:c.3119G>T	NP_001341824.1:p.Arg1040Met
NM_001354896.2:c.3173G>T	NP_001341825.1:p.Arg1058Met
NM_001354897.2:c.3149G>T	NP_001341826.1:p.Arg1050Met
NM_001354898.2:c.3044G>T	NP_001341827.1:p.Arg1015Met
NM_001354899.2:c.3035G>T	NP_001341828.1:p.Arg1012Met
NM_001354900.2:c.2996G>T	NP_001341829.1:p.Arg999Met
NM_001354901.2:c.2942G>T	NP_001341830.1:p.Arg981Met
NM_001354902.2:c.2846G>T	NP_001341831.1:p.Arg949Met
NM_001354903.2:c.2816G>T	NP_001341832.1:p.Arg939Met
NM_001354904.2:c.2741G>T	NP_001341833.1:p.Arg914Met
NM_001354905.2:c.2639G>T	NP_001341834.1:p.Arg880Met
NM_001354906.2:c.2270G>T	NP_001341835.1:p.Arg757Met