Canonical Allele Identifier: CA16028020

Gene: APC

Linked Data

• dbSNP Id: rs1765325527
• MyVariant Identifiers: chr5:g.112174344A>T (hg19) ; chr5:g.112838647A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838647A>T , CM000667.2:g.112838647A>T	GRCh38
NC_000005.9:g.112174344A>T , CM000667.1:g.112174344A>T	GRCh37
NC_000005.8:g.112202243A>T	NCBI36
NG_008481.4:g.151127A>T , LRG_130:g.151127A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2718A>T	ENSP00000484935.2:n.2718A>T
ENST00000504915.3:c.3107A>T	ENSP00000473355.2:p.Asp1036Val
ENST00000505350.2:c.*3059A>T	ENSP00000481752.1:n.*3059A>T
ENST00000507379.6:c.2999A>T	ENSP00000423224.2:p.Asp1000Val
ENST00000509732.6:c.3053A>T	ENSP00000426541.2:p.Asp1018Val
ENST00000512211.7:c.3053A>T	ENSP00000423828.3:p.Asp1018Val
ENST00000257430.9:c.3053A>T MANE Select	ENSP00000257430.4:p.Asp1018Val
ENST00000257430.8:c.3053A>T	ENSP00000257430.4:p.Asp1018Val
ENST00000502371.2:c.1406A>T
ENST00000507379.5:c.2999A>T	ENSP00000423224.1:p.Asp1000Val
ENST00000508376.6:c.3053A>T	ENSP00000427089.2:p.Asp1018Val
ENST00000508624.5:c.*2375A>T	ENSP00000424265.1:n.*2375A>T
ENST00000512211.6:c.3053A>T	ENSP00000423828.2:p.Asp1018Val
ENST00000520401.1:c.230+9675A>T
NM_000038.5:c.3053A>T	NP_000029.2:p.Asp1018Val
NM_001127510.2:c.3053A>T	NP_001120982.1:p.Asp1018Val
NM_001127511.2:c.2999A>T	NP_001120983.2:p.Asp1000Val
NM_001354895.1:c.3053A>T	NP_001341824.1:p.Asp1018Val
NM_001354896.1:c.3107A>T	NP_001341825.1:p.Asp1036Val
NM_001354897.1:c.3083A>T	NP_001341826.1:p.Asp1028Val
NM_001354898.1:c.2978A>T	NP_001341827.1:p.Asp993Val
NM_001354899.1:c.2969A>T	NP_001341828.1:p.Asp990Val
NM_001354900.1:c.2930A>T	NP_001341829.1:p.Asp977Val
NM_001354901.1:c.2876A>T	NP_001341830.1:p.Asp959Val
NM_001354902.1:c.2780A>T	NP_001341831.1:p.Asp927Val
NM_001354903.1:c.2750A>T	NP_001341832.1:p.Asp917Val
NM_001354904.1:c.2675A>T	NP_001341833.1:p.Asp892Val
NM_001354905.1:c.2573A>T	NP_001341834.1:p.Asp858Val
NM_001354906.1:c.2204A>T	NP_001341835.1:p.Asp735Val
NM_000038.6:c.3053A>T MANE Select	NP_000029.2:p.Asp1018Val
NM_001127510.3:c.3053A>T	NP_001120982.1:p.Asp1018Val
NM_001127511.3:c.2999A>T	NP_001120983.2:p.Asp1000Val
NM_001354895.2:c.3053A>T	NP_001341824.1:p.Asp1018Val
NM_001354896.2:c.3107A>T	NP_001341825.1:p.Asp1036Val
NM_001354897.2:c.3083A>T	NP_001341826.1:p.Asp1028Val
NM_001354898.2:c.2978A>T	NP_001341827.1:p.Asp993Val
NM_001354899.2:c.2969A>T	NP_001341828.1:p.Asp990Val
NM_001354900.2:c.2930A>T	NP_001341829.1:p.Asp977Val
NM_001354901.2:c.2876A>T	NP_001341830.1:p.Asp959Val
NM_001354902.2:c.2780A>T	NP_001341831.1:p.Asp927Val
NM_001354903.2:c.2750A>T	NP_001341832.1:p.Asp917Val
NM_001354904.2:c.2675A>T	NP_001341833.1:p.Asp892Val
NM_001354905.2:c.2573A>T	NP_001341834.1:p.Asp858Val
NM_001354906.2:c.2204A>T	NP_001341835.1:p.Asp735Val