Canonical Allele Identifier: CA10582282

Gene: APC

Linked Data

• ClinVar Variation Id: 236652
• ClinVar RCV Id: RCV001027222
• dbSNP Id: rs878853473
• MyVariant Identifiers: chr5:g.112137060G>C (hg19) ; chr5:g.112801363G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112801363G>C , CM000667.2:g.112801363G>C	GRCh38
NC_000005.9:g.112137060G>C , CM000667.1:g.112137060G>C	GRCh37
NC_000005.8:g.112164959G>C	NCBI36
NG_008481.4:g.113843G>C , LRG_130:g.113843G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.814G>C	ENSP00000484935.2:p.Ala272Pro
ENST00000504915.3:c.814G>C	ENSP00000473355.2:p.Ala272Pro
ENST00000505084.2:n.870G>C
ENST00000505350.2:c.*820G>C	ENSP00000481752.1:n.*820G>C
ENST00000507379.6:c.760G>C	ENSP00000423224.2:p.Ala254Pro
ENST00000509732.6:c.814G>C	ENSP00000426541.2:p.Ala272Pro
ENST00000512211.7:c.814G>C	ENSP00000423828.3:p.Ala272Pro
ENST00000257430.9:c.814G>C MANE Select	ENSP00000257430.4:p.Ala272Pro
ENST00000257430.8:c.814G>C	ENSP00000257430.4:p.Ala272Pro
ENST00000507379.5:c.760G>C	ENSP00000423224.1:p.Ala254Pro
ENST00000508376.6:c.814G>C	ENSP00000427089.2:p.Ala272Pro
ENST00000508624.5:c.814G>C	ENSP00000424265.1:p.Ala272Pro
ENST00000512211.6:c.814G>C	ENSP00000423828.2:p.Ala272Pro
NM_000038.5:c.814G>C	NP_000029.2:p.Ala272Pro
NM_001127510.2:c.814G>C	NP_001120982.1:p.Ala272Pro
NM_001127511.2:c.760G>C	NP_001120983.2:p.Ala254Pro
NM_001354895.1:c.814G>C	NP_001341824.1:p.Ala272Pro
NM_001354896.1:c.814G>C	NP_001341825.1:p.Ala272Pro
NM_001354897.1:c.844G>C	NP_001341826.1:p.Ala282Pro
NM_001354898.1:c.739G>C	NP_001341827.1:p.Ala247Pro
NM_001354899.1:c.730G>C	NP_001341828.1:p.Ala244Pro
NM_001354900.1:c.637G>C	NP_001341829.1:p.Ala213Pro
NM_001354901.1:c.637G>C	NP_001341830.1:p.Ala213Pro
NM_001354902.1:c.844G>C	NP_001341831.1:p.Ala282Pro
NM_001354903.1:c.814G>C	NP_001341832.1:p.Ala272Pro
NM_001354904.1:c.739G>C	NP_001341833.1:p.Ala247Pro
NM_001354905.1:c.637G>C	NP_001341834.1:p.Ala213Pro
NM_001354906.1:c.-222G>C	NP_001341835.1:n.-222G>C
NM_000038.6:c.814G>C MANE Select	NP_000029.2:p.Ala272Pro
NM_001127510.3:c.814G>C	NP_001120982.1:p.Ala272Pro
NM_001127511.3:c.760G>C	NP_001120983.2:p.Ala254Pro
NM_001354895.2:c.814G>C	NP_001341824.1:p.Ala272Pro
NM_001354896.2:c.814G>C	NP_001341825.1:p.Ala272Pro
NM_001354897.2:c.844G>C	NP_001341826.1:p.Ala282Pro
NM_001354898.2:c.739G>C	NP_001341827.1:p.Ala247Pro
NM_001354899.2:c.730G>C	NP_001341828.1:p.Ala244Pro
NM_001354900.2:c.637G>C	NP_001341829.1:p.Ala213Pro
NM_001354901.2:c.637G>C	NP_001341830.1:p.Ala213Pro
NM_001354902.2:c.844G>C	NP_001341831.1:p.Ala282Pro
NM_001354903.2:c.814G>C	NP_001341832.1:p.Ala272Pro
NM_001354904.2:c.739G>C	NP_001341833.1:p.Ala247Pro
NM_001354905.2:c.637G>C	NP_001341834.1:p.Ala213Pro
NM_001354906.2:c.-222G>C	NP_001341835.1:n.-222G>C