Canonical Allele Identifier: CA445963543

Gene: APC

Linked Data

• dbSNP Id: rs2149893468
• MyVariant Identifiers: chr5:g.112174804T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839107T>G , CM000667.2:g.112839107T>G	GRCh38
NC_000005.9:g.112174804T>G , CM000667.1:g.112174804T>G	GRCh37
NC_000005.8:g.112202703T>G	NCBI36
NG_008481.4:g.151587T>G , LRG_130:g.151587T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3178T>G	ENSP00000484935.2:n.3178T>G
ENST00000504915.3:c.3567T>G	ENSP00000473355.2:p.Arg1189=
ENST00000505350.2:c.*3519T>G	ENSP00000481752.1:n.*3519T>G
ENST00000507379.6:c.3459T>G	ENSP00000423224.2:p.Arg1153=
ENST00000509732.6:c.3513T>G	ENSP00000426541.2:p.Arg1171=
ENST00000512211.7:c.3513T>G	ENSP00000423828.3:p.Arg1171=
ENST00000257430.9:c.3513T>G MANE Select	ENSP00000257430.4:p.Arg1171=
ENST00000257430.8:c.3513T>G	ENSP00000257430.4:p.Arg1171=
ENST00000502371.2:c.1866T>G
ENST00000508376.6:c.3513T>G	ENSP00000427089.2:p.Arg1171=
ENST00000508624.5:c.*2835T>G	ENSP00000424265.1:n.*2835T>G
ENST00000512211.6:c.3513T>G	ENSP00000423828.2:p.Arg1171=
ENST00000520401.1:c.230+10135T>G
NM_000038.5:c.3513T>G	NP_000029.2:p.Arg1171=
NM_001127510.2:c.3513T>G	NP_001120982.1:p.Arg1171=
NM_001127511.2:c.3459T>G	NP_001120983.2:p.Arg1153=
NM_001354895.1:c.3513T>G	NP_001341824.1:p.Arg1171=
NM_001354896.1:c.3567T>G	NP_001341825.1:p.Arg1189=
NM_001354897.1:c.3543T>G	NP_001341826.1:p.Arg1181=
NM_001354898.1:c.3438T>G	NP_001341827.1:p.Arg1146=
NM_001354899.1:c.3429T>G	NP_001341828.1:p.Arg1143=
NM_001354900.1:c.3390T>G	NP_001341829.1:p.Arg1130=
NM_001354901.1:c.3336T>G	NP_001341830.1:p.Arg1112=
NM_001354902.1:c.3240T>G	NP_001341831.1:p.Arg1080=
NM_001354903.1:c.3210T>G	NP_001341832.1:p.Arg1070=
NM_001354904.1:c.3135T>G	NP_001341833.1:p.Arg1045=
NM_001354905.1:c.3033T>G	NP_001341834.1:p.Arg1011=
NM_001354906.1:c.2664T>G	NP_001341835.1:p.Arg888=
NM_000038.6:c.3513T>G MANE Select	NP_000029.2:p.Arg1171=
NM_001127510.3:c.3513T>G	NP_001120982.1:p.Arg1171=
NM_001127511.3:c.3459T>G	NP_001120983.2:p.Arg1153=
NM_001354895.2:c.3513T>G	NP_001341824.1:p.Arg1171=
NM_001354896.2:c.3567T>G	NP_001341825.1:p.Arg1189=
NM_001354897.2:c.3543T>G	NP_001341826.1:p.Arg1181=
NM_001354898.2:c.3438T>G	NP_001341827.1:p.Arg1146=
NM_001354899.2:c.3429T>G	NP_001341828.1:p.Arg1143=
NM_001354900.2:c.3390T>G	NP_001341829.1:p.Arg1130=
NM_001354901.2:c.3336T>G	NP_001341830.1:p.Arg1112=
NM_001354902.2:c.3240T>G	NP_001341831.1:p.Arg1080=
NM_001354903.2:c.3210T>G	NP_001341832.1:p.Arg1070=
NM_001354904.2:c.3135T>G	NP_001341833.1:p.Arg1045=
NM_001354905.2:c.3033T>G	NP_001341834.1:p.Arg1011=
NM_001354906.2:c.2664T>G	NP_001341835.1:p.Arg888=