Canonical Allele Identifier: CA16030313

Gene: APC

Linked Data

• dbSNP Id: rs761886683
• MyVariant Identifiers: chr5:g.112175392G>T (hg19) ; chr5:g.112839695G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839695G>T , CM000667.2:g.112839695G>T	GRCh38
NC_000005.9:g.112175392G>T , CM000667.1:g.112175392G>T	GRCh37
NC_000005.8:g.112203291G>T	NCBI36
NG_008481.4:g.152175G>T , LRG_130:g.152175G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3766G>T	ENSP00000484935.2:n.3766G>T
ENST00000504915.3:c.4155G>T	ENSP00000473355.2:p.Gln1385His
ENST00000505350.2:c.*4107G>T	ENSP00000481752.1:n.*4107G>T
ENST00000507379.6:c.4047G>T	ENSP00000423224.2:p.Gln1349His
ENST00000509732.6:c.4101G>T	ENSP00000426541.2:p.Gln1367His
ENST00000512211.7:c.4101G>T	ENSP00000423828.3:p.Gln1367His
ENST00000257430.9:c.4101G>T MANE Select	ENSP00000257430.4:p.Gln1367His
ENST00000257430.8:c.4101G>T	ENSP00000257430.4:p.Gln1367His
ENST00000502371.2:c.2454G>T
ENST00000508376.6:c.4101G>T	ENSP00000427089.2:p.Gln1367His
ENST00000508624.5:c.*3423G>T	ENSP00000424265.1:n.*3423G>T
ENST00000520401.1:c.230+10723G>T
NM_000038.5:c.4101G>T	NP_000029.2:p.Gln1367His
NM_001127510.2:c.4101G>T	NP_001120982.1:p.Gln1367His
NM_001127511.2:c.4047G>T	NP_001120983.2:p.Gln1349His
NM_001354895.1:c.4101G>T	NP_001341824.1:p.Gln1367His
NM_001354896.1:c.4155G>T	NP_001341825.1:p.Gln1385His
NM_001354897.1:c.4131G>T	NP_001341826.1:p.Gln1377His
NM_001354898.1:c.4026G>T	NP_001341827.1:p.Gln1342His
NM_001354899.1:c.4017G>T	NP_001341828.1:p.Gln1339His
NM_001354900.1:c.3978G>T	NP_001341829.1:p.Gln1326His
NM_001354901.1:c.3924G>T	NP_001341830.1:p.Gln1308His
NM_001354902.1:c.3828G>T	NP_001341831.1:p.Gln1276His
NM_001354903.1:c.3798G>T	NP_001341832.1:p.Gln1266His
NM_001354904.1:c.3723G>T	NP_001341833.1:p.Gln1241His
NM_001354905.1:c.3621G>T	NP_001341834.1:p.Gln1207His
NM_001354906.1:c.3252G>T	NP_001341835.1:p.Gln1084His
NM_000038.6:c.4101G>T MANE Select	NP_000029.2:p.Gln1367His
NM_001127510.3:c.4101G>T	NP_001120982.1:p.Gln1367His
NM_001127511.3:c.4047G>T	NP_001120983.2:p.Gln1349His
NM_001354895.2:c.4101G>T	NP_001341824.1:p.Gln1367His
NM_001354896.2:c.4155G>T	NP_001341825.1:p.Gln1385His
NM_001354897.2:c.4131G>T	NP_001341826.1:p.Gln1377His
NM_001354898.2:c.4026G>T	NP_001341827.1:p.Gln1342His
NM_001354899.2:c.4017G>T	NP_001341828.1:p.Gln1339His
NM_001354900.2:c.3978G>T	NP_001341829.1:p.Gln1326His
NM_001354901.2:c.3924G>T	NP_001341830.1:p.Gln1308His
NM_001354902.2:c.3828G>T	NP_001341831.1:p.Gln1276His
NM_001354903.2:c.3798G>T	NP_001341832.1:p.Gln1266His
NM_001354904.2:c.3723G>T	NP_001341833.1:p.Gln1241His
NM_001354905.2:c.3621G>T	NP_001341834.1:p.Gln1207His
NM_001354906.2:c.3252G>T	NP_001341835.1:p.Gln1084His