Canonical Allele Identifier: CA446211040

Gene: APC

Linked Data

• dbSNP Id: rs1186346278
• MyVariant Identifiers: chr5:g.112179337G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843640G>C , CM000667.2:g.112843640G>C	GRCh38
NC_000005.9:g.112179337G>C , CM000667.1:g.112179337G>C	GRCh37
NC_000005.8:g.112207236G>C	NCBI36
NG_008481.4:g.156120G>C , LRG_130:g.156120G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.8100G>C	ENSP00000473355.2:p.Val2700=
ENST00000505350.2:c.*8052G>C	ENSP00000481752.1:n.*8052G>C
ENST00000507379.6:c.7992G>C	ENSP00000423224.2:p.Val2664=
ENST00000509732.6:c.8046G>C	ENSP00000426541.2:p.Val2682=
ENST00000512211.7:c.8046G>C	ENSP00000423828.3:p.Val2682=
ENST00000257430.9:c.8046G>C MANE Select	ENSP00000257430.4:p.Val2682=
ENST00000257430.8:c.8046G>C	ENSP00000257430.4:p.Val2682=
ENST00000508376.6:c.8046G>C	ENSP00000427089.2:p.Val2682=
ENST00000520401.1:c.231-13009G>C
NM_000038.5:c.8046G>C	NP_000029.2:p.Val2682=
NM_001127510.2:c.8046G>C	NP_001120982.1:p.Val2682=
NM_001127511.2:c.7992G>C	NP_001120983.2:p.Val2664=
NM_001354895.1:c.8046G>C	NP_001341824.1:p.Val2682=
NM_001354896.1:c.8100G>C	NP_001341825.1:p.Val2700=
NM_001354897.1:c.8076G>C	NP_001341826.1:p.Val2692=
NM_001354898.1:c.7971G>C	NP_001341827.1:p.Val2657=
NM_001354899.1:c.7962G>C	NP_001341828.1:p.Val2654=
NM_001354900.1:c.7923G>C	NP_001341829.1:p.Val2641=
NM_001354901.1:c.7869G>C	NP_001341830.1:p.Val2623=
NM_001354902.1:c.7773G>C	NP_001341831.1:p.Val2591=
NM_001354903.1:c.7743G>C	NP_001341832.1:p.Val2581=
NM_001354904.1:c.7668G>C	NP_001341833.1:p.Val2556=
NM_001354905.1:c.7566G>C	NP_001341834.1:p.Val2522=
NM_001354906.1:c.7197G>C	NP_001341835.1:p.Val2399=
NM_000038.6:c.8046G>C MANE Select	NP_000029.2:p.Val2682=
NM_001127510.3:c.8046G>C	NP_001120982.1:p.Val2682=
NM_001127511.3:c.7992G>C	NP_001120983.2:p.Val2664=
NM_001354895.2:c.8046G>C	NP_001341824.1:p.Val2682=
NM_001354896.2:c.8100G>C	NP_001341825.1:p.Val2700=
NM_001354897.2:c.8076G>C	NP_001341826.1:p.Val2692=
NM_001354898.2:c.7971G>C	NP_001341827.1:p.Val2657=
NM_001354899.2:c.7962G>C	NP_001341828.1:p.Val2654=
NM_001354900.2:c.7923G>C	NP_001341829.1:p.Val2641=
NM_001354901.2:c.7869G>C	NP_001341830.1:p.Val2623=
NM_001354902.2:c.7773G>C	NP_001341831.1:p.Val2591=
NM_001354903.2:c.7743G>C	NP_001341832.1:p.Val2581=
NM_001354904.2:c.7668G>C	NP_001341833.1:p.Val2556=
NM_001354905.2:c.7566G>C	NP_001341834.1:p.Val2522=
NM_001354906.2:c.7197G>C	NP_001341835.1:p.Val2399=