Canonical Allele Identifier: CA16029910

Gene: APC

Linked Data

• dbSNP Id: rs746289994
• MyVariant Identifiers: chr5:g.112175200A>T (hg19) ; chr5:g.112839503A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839503A>T , CM000667.2:g.112839503A>T	GRCh38
NC_000005.9:g.112175200A>T , CM000667.1:g.112175200A>T	GRCh37
NC_000005.8:g.112203099A>T	NCBI36
NG_008481.4:g.151983A>T , LRG_130:g.151983A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3574A>T	ENSP00000484935.2:n.3574A>T
ENST00000504915.3:c.3963A>T	ENSP00000473355.2:p.Gln1321His
ENST00000505350.2:c.*3915A>T	ENSP00000481752.1:n.*3915A>T
ENST00000507379.6:c.3855A>T	ENSP00000423224.2:p.Gln1285His
ENST00000509732.6:c.3909A>T	ENSP00000426541.2:p.Gln1303His
ENST00000512211.7:c.3909A>T	ENSP00000423828.3:p.Gln1303His
ENST00000257430.9:c.3909A>T MANE Select	ENSP00000257430.4:p.Gln1303His
ENST00000257430.8:c.3909A>T	ENSP00000257430.4:p.Gln1303His
ENST00000502371.2:c.2262A>T
ENST00000508376.6:c.3909A>T	ENSP00000427089.2:p.Gln1303His
ENST00000508624.5:c.*3231A>T	ENSP00000424265.1:n.*3231A>T
ENST00000512211.6:c.3909A>T	ENSP00000423828.2:p.Gln1303His
ENST00000520401.1:c.230+10531A>T
NM_000038.5:c.3909A>T	NP_000029.2:p.Gln1303His
NM_001127510.2:c.3909A>T	NP_001120982.1:p.Gln1303His
NM_001127511.2:c.3855A>T	NP_001120983.2:p.Gln1285His
NM_001354895.1:c.3909A>T	NP_001341824.1:p.Gln1303His
NM_001354896.1:c.3963A>T	NP_001341825.1:p.Gln1321His
NM_001354897.1:c.3939A>T	NP_001341826.1:p.Gln1313His
NM_001354898.1:c.3834A>T	NP_001341827.1:p.Gln1278His
NM_001354899.1:c.3825A>T	NP_001341828.1:p.Gln1275His
NM_001354900.1:c.3786A>T	NP_001341829.1:p.Gln1262His
NM_001354901.1:c.3732A>T	NP_001341830.1:p.Gln1244His
NM_001354902.1:c.3636A>T	NP_001341831.1:p.Gln1212His
NM_001354903.1:c.3606A>T	NP_001341832.1:p.Gln1202His
NM_001354904.1:c.3531A>T	NP_001341833.1:p.Gln1177His
NM_001354905.1:c.3429A>T	NP_001341834.1:p.Gln1143His
NM_001354906.1:c.3060A>T	NP_001341835.1:p.Gln1020His
NM_000038.6:c.3909A>T MANE Select	NP_000029.2:p.Gln1303His
NM_001127510.3:c.3909A>T	NP_001120982.1:p.Gln1303His
NM_001127511.3:c.3855A>T	NP_001120983.2:p.Gln1285His
NM_001354895.2:c.3909A>T	NP_001341824.1:p.Gln1303His
NM_001354896.2:c.3963A>T	NP_001341825.1:p.Gln1321His
NM_001354897.2:c.3939A>T	NP_001341826.1:p.Gln1313His
NM_001354898.2:c.3834A>T	NP_001341827.1:p.Gln1278His
NM_001354899.2:c.3825A>T	NP_001341828.1:p.Gln1275His
NM_001354900.2:c.3786A>T	NP_001341829.1:p.Gln1262His
NM_001354901.2:c.3732A>T	NP_001341830.1:p.Gln1244His
NM_001354902.2:c.3636A>T	NP_001341831.1:p.Gln1212His
NM_001354903.2:c.3606A>T	NP_001341832.1:p.Gln1202His
NM_001354904.2:c.3531A>T	NP_001341833.1:p.Gln1177His
NM_001354905.2:c.3429A>T	NP_001341834.1:p.Gln1143His
NM_001354906.2:c.3060A>T	NP_001341835.1:p.Gln1020His