Canonical Allele Identifier: CA007680

Gene: APC

Linked Data

• ClinVar Variation Id: 135692
• ClinVar RCV Id: RCV000122766 ; RCV000413883 ; RCV000566722 ; RCV002228421
• dbSNP Id: rs587780592
• ExAC: 5:112102928 G / A
• gnomAD v2: 5-112102928-G-A
• gnomAD v3: 5-112767231-G-A
• gnomAD v4: 5-112767231-G-A
• MyVariant Identifiers: chr5:g.112102928G>A (hg19) ; chr5:g.112767231G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112767231G>A , CM000667.2:g.112767231G>A	GRCh38
NC_000005.9:g.112102928G>A , CM000667.1:g.112102928G>A	GRCh37
NC_000005.8:g.112130827G>A	NCBI36
NG_008481.4:g.79711G>A , LRG_130:g.79711G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.263G>A	ENSP00000484935.2:p.Arg88Gln
ENST00000504915.3:c.263G>A	ENSP00000473355.2:p.Arg88Gln
ENST00000505084.2:n.319G>A
ENST00000505350.2:c.*269G>A	ENSP00000481752.1:n.*269G>A
ENST00000507379.6:c.293G>A	ENSP00000423224.2:p.Arg98Gln
ENST00000509732.6:c.263G>A	ENSP00000426541.2:p.Arg88Gln
ENST00000512211.7:c.263G>A	ENSP00000423828.3:p.Arg88Gln
ENST00000257430.9:c.263G>A MANE Select	ENSP00000257430.4:p.Arg88Gln
ENST00000257430.8:c.263G>A	ENSP00000257430.4:p.Arg88Gln
ENST00000507379.5:c.293G>A	ENSP00000423224.1:p.Arg98Gln
ENST00000508376.6:c.263G>A	ENSP00000427089.2:p.Arg88Gln
ENST00000508624.5:c.263G>A	ENSP00000424265.1:p.Arg88Gln
ENST00000509732.5:c.263G>A	ENSP00000426541.1:p.Arg88Gln
ENST00000512211.6:c.263G>A	ENSP00000423828.2:p.Arg88Gln
NM_000038.5:c.263G>A	NP_000029.2:p.Arg88Gln
NM_001127510.2:c.263G>A	NP_001120982.1:p.Arg88Gln
NM_001127511.2:c.293G>A	NP_001120983.2:p.Arg98Gln
NM_001354895.1:c.263G>A	NP_001341824.1:p.Arg88Gln
NM_001354896.1:c.263G>A	NP_001341825.1:p.Arg88Gln
NM_001354897.1:c.293G>A	NP_001341826.1:p.Arg98Gln
NM_001354898.1:c.188G>A	NP_001341827.1:p.Arg63Gln
NM_001354899.1:c.263G>A	NP_001341828.1:p.Arg88Gln
NM_001354900.1:c.86G>A	NP_001341829.1:p.Arg29Gln
NM_001354901.1:c.86G>A	NP_001341830.1:p.Arg29Gln
NM_001354902.1:c.293G>A	NP_001341831.1:p.Arg98Gln
NM_001354903.1:c.263G>A	NP_001341832.1:p.Arg88Gln
NM_001354904.1:c.188G>A	NP_001341833.1:p.Arg63Gln
NM_001354905.1:c.86G>A	NP_001341834.1:p.Arg29Gln
NM_001354906.1:c.-773G>A	NP_001341835.1:n.-773G>A
NM_000038.6:c.263G>A MANE Select	NP_000029.2:p.Arg88Gln
NM_001127510.3:c.263G>A	NP_001120982.1:p.Arg88Gln
NM_001127511.3:c.293G>A	NP_001120983.2:p.Arg98Gln
NM_001354895.2:c.263G>A	NP_001341824.1:p.Arg88Gln
NM_001354896.2:c.263G>A	NP_001341825.1:p.Arg88Gln
NM_001354897.2:c.293G>A	NP_001341826.1:p.Arg98Gln
NM_001354898.2:c.188G>A	NP_001341827.1:p.Arg63Gln
NM_001354899.2:c.263G>A	NP_001341828.1:p.Arg88Gln
NM_001354900.2:c.86G>A	NP_001341829.1:p.Arg29Gln
NM_001354901.2:c.86G>A	NP_001341830.1:p.Arg29Gln
NM_001354902.2:c.293G>A	NP_001341831.1:p.Arg98Gln
NM_001354903.2:c.263G>A	NP_001341832.1:p.Arg88Gln
NM_001354904.2:c.188G>A	NP_001341833.1:p.Arg63Gln
NM_001354905.2:c.86G>A	NP_001341834.1:p.Arg29Gln
NM_001354906.2:c.-773G>A	NP_001341835.1:n.-773G>A