Canonical Allele Identifier: CA445758914

Gene: APC

Linked Data

• ClinVar Variation Id: 1782364
• ClinVar RCV Id: RCV002408319 ; RCV004060786
• MyVariant Identifiers: chr5:g.112170809A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835112A>C , CM000667.2:g.112835112A>C	GRCh38
NC_000005.9:g.112170809A>C , CM000667.1:g.112170809A>C	GRCh37
NC_000005.8:g.112198708A>C	NCBI36
NG_008481.4:g.147592A>C , LRG_130:g.147592A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1570A>C	ENSP00000484935.2:n.1570A>C
ENST00000504915.3:c.1959A>C	ENSP00000473355.2:p.Gly653=
ENST00000505350.2:c.*1911A>C	ENSP00000481752.1:n.*1911A>C
ENST00000507379.6:c.1851A>C	ENSP00000423224.2:p.Gly617=
ENST00000509732.6:c.1905A>C	ENSP00000426541.2:p.Gly635=
ENST00000512211.7:c.1905A>C	ENSP00000423828.3:p.Gly635=
ENST00000257430.9:c.1905A>C MANE Select	ENSP00000257430.4:p.Gly635=
ENST00000257430.8:c.1905A>C	ENSP00000257430.4:p.Gly635=
ENST00000502371.2:c.258A>C
ENST00000504915.2:c.594A>C	ENSP00000473355.1:p.Gly198=
ENST00000507379.5:c.1851A>C	ENSP00000423224.1:p.Gly617=
ENST00000508376.6:c.1905A>C	ENSP00000427089.2:p.Gly635=
ENST00000508624.5:c.*1227A>C	ENSP00000424265.1:n.*1227A>C
ENST00000512211.6:c.1905A>C	ENSP00000423828.2:p.Gly635=
ENST00000520401.1:c.230+6140A>C
NM_000038.5:c.1905A>C	NP_000029.2:p.Gly635=
NM_001127510.2:c.1905A>C	NP_001120982.1:p.Gly635=
NM_001127511.2:c.1851A>C	NP_001120983.2:p.Gly617=
NM_001354895.1:c.1905A>C	NP_001341824.1:p.Gly635=
NM_001354896.1:c.1959A>C	NP_001341825.1:p.Gly653=
NM_001354897.1:c.1935A>C	NP_001341826.1:p.Gly645=
NM_001354898.1:c.1830A>C	NP_001341827.1:p.Gly610=
NM_001354899.1:c.1821A>C	NP_001341828.1:p.Gly607=
NM_001354900.1:c.1782A>C	NP_001341829.1:p.Gly594=
NM_001354901.1:c.1728A>C	NP_001341830.1:p.Gly576=
NM_001354902.1:c.1632A>C	NP_001341831.1:p.Gly544=
NM_001354903.1:c.1602A>C	NP_001341832.1:p.Gly534=
NM_001354904.1:c.1527A>C	NP_001341833.1:p.Gly509=
NM_001354905.1:c.1425A>C	NP_001341834.1:p.Gly475=
NM_001354906.1:c.1056A>C	NP_001341835.1:p.Gly352=
NM_000038.6:c.1905A>C MANE Select	NP_000029.2:p.Gly635=
NM_001127510.3:c.1905A>C	NP_001120982.1:p.Gly635=
NM_001127511.3:c.1851A>C	NP_001120983.2:p.Gly617=
NM_001354895.2:c.1905A>C	NP_001341824.1:p.Gly635=
NM_001354896.2:c.1959A>C	NP_001341825.1:p.Gly653=
NM_001354897.2:c.1935A>C	NP_001341826.1:p.Gly645=
NM_001354898.2:c.1830A>C	NP_001341827.1:p.Gly610=
NM_001354899.2:c.1821A>C	NP_001341828.1:p.Gly607=
NM_001354900.2:c.1782A>C	NP_001341829.1:p.Gly594=
NM_001354901.2:c.1728A>C	NP_001341830.1:p.Gly576=
NM_001354902.2:c.1632A>C	NP_001341831.1:p.Gly544=
NM_001354903.2:c.1602A>C	NP_001341832.1:p.Gly534=
NM_001354904.2:c.1527A>C	NP_001341833.1:p.Gly509=
NM_001354905.2:c.1425A>C	NP_001341834.1:p.Gly475=
NM_001354906.2:c.1056A>C	NP_001341835.1:p.Gly352=