Canonical Allele Identifier: CA16028036

Gene: APC

Linked Data

• ClinVar Variation Id: 1799369
• ClinVar RCV Id: RCV002444216
• dbSNP Id: rs1057522595
• MyVariant Identifiers: chr5:g.112174351A>T (hg19) ; chr5:g.112838654A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838654A>T , CM000667.2:g.112838654A>T	GRCh38
NC_000005.9:g.112174351A>T , CM000667.1:g.112174351A>T	GRCh37
NC_000005.8:g.112202250A>T	NCBI36
NG_008481.4:g.151134A>T , LRG_130:g.151134A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2725A>T	ENSP00000484935.2:n.2725A>T
ENST00000504915.3:c.3114A>T	ENSP00000473355.2:p.Glu1038Asp
ENST00000505350.2:c.*3066A>T	ENSP00000481752.1:n.*3066A>T
ENST00000507379.6:c.3006A>T	ENSP00000423224.2:p.Glu1002Asp
ENST00000509732.6:c.3060A>T	ENSP00000426541.2:p.Glu1020Asp
ENST00000512211.7:c.3060A>T	ENSP00000423828.3:p.Glu1020Asp
ENST00000257430.9:c.3060A>T MANE Select	ENSP00000257430.4:p.Glu1020Asp
ENST00000257430.8:c.3060A>T	ENSP00000257430.4:p.Glu1020Asp
ENST00000502371.2:c.1413A>T
ENST00000507379.5:c.3006A>T	ENSP00000423224.1:p.Glu1002Asp
ENST00000508376.6:c.3060A>T	ENSP00000427089.2:p.Glu1020Asp
ENST00000508624.5:c.*2382A>T	ENSP00000424265.1:n.*2382A>T
ENST00000512211.6:c.3060A>T	ENSP00000423828.2:p.Glu1020Asp
ENST00000520401.1:c.230+9682A>T
NM_000038.5:c.3060A>T	NP_000029.2:p.Glu1020Asp
NM_001127510.2:c.3060A>T	NP_001120982.1:p.Glu1020Asp
NM_001127511.2:c.3006A>T	NP_001120983.2:p.Glu1002Asp
NM_001354895.1:c.3060A>T	NP_001341824.1:p.Glu1020Asp
NM_001354896.1:c.3114A>T	NP_001341825.1:p.Glu1038Asp
NM_001354897.1:c.3090A>T	NP_001341826.1:p.Glu1030Asp
NM_001354898.1:c.2985A>T	NP_001341827.1:p.Glu995Asp
NM_001354899.1:c.2976A>T	NP_001341828.1:p.Glu992Asp
NM_001354900.1:c.2937A>T	NP_001341829.1:p.Glu979Asp
NM_001354901.1:c.2883A>T	NP_001341830.1:p.Glu961Asp
NM_001354902.1:c.2787A>T	NP_001341831.1:p.Glu929Asp
NM_001354903.1:c.2757A>T	NP_001341832.1:p.Glu919Asp
NM_001354904.1:c.2682A>T	NP_001341833.1:p.Glu894Asp
NM_001354905.1:c.2580A>T	NP_001341834.1:p.Glu860Asp
NM_001354906.1:c.2211A>T	NP_001341835.1:p.Glu737Asp
NM_000038.6:c.3060A>T MANE Select	NP_000029.2:p.Glu1020Asp
NM_001127510.3:c.3060A>T	NP_001120982.1:p.Glu1020Asp
NM_001127511.3:c.3006A>T	NP_001120983.2:p.Glu1002Asp
NM_001354895.2:c.3060A>T	NP_001341824.1:p.Glu1020Asp
NM_001354896.2:c.3114A>T	NP_001341825.1:p.Glu1038Asp
NM_001354897.2:c.3090A>T	NP_001341826.1:p.Glu1030Asp
NM_001354898.2:c.2985A>T	NP_001341827.1:p.Glu995Asp
NM_001354899.2:c.2976A>T	NP_001341828.1:p.Glu992Asp
NM_001354900.2:c.2937A>T	NP_001341829.1:p.Glu979Asp
NM_001354901.2:c.2883A>T	NP_001341830.1:p.Glu961Asp
NM_001354902.2:c.2787A>T	NP_001341831.1:p.Glu929Asp
NM_001354903.2:c.2757A>T	NP_001341832.1:p.Glu919Asp
NM_001354904.2:c.2682A>T	NP_001341833.1:p.Glu894Asp
NM_001354905.2:c.2580A>T	NP_001341834.1:p.Glu860Asp
NM_001354906.2:c.2211A>T	NP_001341835.1:p.Glu737Asp