Canonical Allele Identifier: CA445757372

Gene: APC

Linked Data

• dbSNP Id: rs351771
• MyVariant Identifiers: chr5:g.112164561G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828864G>C , CM000667.2:g.112828864G>C	GRCh38
NC_000005.9:g.112164561G>C , CM000667.1:g.112164561G>C	GRCh37
NC_000005.8:g.112192460G>C	NCBI36
NG_008481.4:g.141344G>C , LRG_130:g.141344G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1409-6087G>C	ENSP00000484935.2:n.1409-6087G>C
ENST00000504915.3:c.1689G>C	ENSP00000473355.2:p.Ala563=
ENST00000505084.2:n.1691G>C
ENST00000505350.2:c.*1641G>C	ENSP00000481752.1:n.*1641G>C
ENST00000507379.6:c.1581G>C	ENSP00000423224.2:p.Ala527=
ENST00000509732.6:c.1635G>C	ENSP00000426541.2:p.Ala545=
ENST00000512211.7:c.1635G>C	ENSP00000423828.3:p.Ala545=
ENST00000257430.9:c.1635G>C MANE Select	ENSP00000257430.4:p.Ala545=
ENST00000257430.8:c.1635G>C	ENSP00000257430.4:p.Ala545=
ENST00000502371.2:c.97-6087G>C
ENST00000504915.2:c.324G>C	ENSP00000473355.1:p.Ala108=
ENST00000505084.1:n.122G>C
ENST00000507379.5:c.1581G>C	ENSP00000423224.1:p.Ala527=
ENST00000508376.6:c.1635G>C	ENSP00000427089.2:p.Ala545=
ENST00000508624.5:c.*957G>C	ENSP00000424265.1:n.*957G>C
ENST00000512211.6:c.1635G>C	ENSP00000423828.2:p.Ala545=
ENST00000520401.1:c.122G>C
NM_000038.5:c.1635G>C	NP_000029.2:p.Ala545=
NM_001127510.2:c.1635G>C	NP_001120982.1:p.Ala545=
NM_001127511.2:c.1581G>C	NP_001120983.2:p.Ala527=
NM_001354895.1:c.1635G>C	NP_001341824.1:p.Ala545=
NM_001354896.1:c.1689G>C	NP_001341825.1:p.Ala563=
NM_001354897.1:c.1665G>C	NP_001341826.1:p.Ala555=
NM_001354898.1:c.1560G>C	NP_001341827.1:p.Ala520=
NM_001354899.1:c.1551G>C	NP_001341828.1:p.Ala517=
NM_001354900.1:c.1512G>C	NP_001341829.1:p.Ala504=
NM_001354901.1:c.1458G>C	NP_001341830.1:p.Ala486=
NM_001354902.1:c.1362G>C	NP_001341831.1:p.Ala454=
NM_001354903.1:c.1332G>C	NP_001341832.1:p.Ala444=
NM_001354904.1:c.1257G>C	NP_001341833.1:p.Ala419=
NM_001354905.1:c.1155G>C	NP_001341834.1:p.Ala385=
NM_001354906.1:c.786G>C	NP_001341835.1:p.Ala262=
NM_000038.6:c.1635G>C MANE Select	NP_000029.2:p.Ala545=
NM_001127510.3:c.1635G>C	NP_001120982.1:p.Ala545=
NM_001127511.3:c.1581G>C	NP_001120983.2:p.Ala527=
NM_001354895.2:c.1635G>C	NP_001341824.1:p.Ala545=
NM_001354896.2:c.1689G>C	NP_001341825.1:p.Ala563=
NM_001354897.2:c.1665G>C	NP_001341826.1:p.Ala555=
NM_001354898.2:c.1560G>C	NP_001341827.1:p.Ala520=
NM_001354899.2:c.1551G>C	NP_001341828.1:p.Ala517=
NM_001354900.2:c.1512G>C	NP_001341829.1:p.Ala504=
NM_001354901.2:c.1458G>C	NP_001341830.1:p.Ala486=
NM_001354902.2:c.1362G>C	NP_001341831.1:p.Ala454=
NM_001354903.2:c.1332G>C	NP_001341832.1:p.Ala444=
NM_001354904.2:c.1257G>C	NP_001341833.1:p.Ala419=
NM_001354905.2:c.1155G>C	NP_001341834.1:p.Ala385=
NM_001354906.2:c.786G>C	NP_001341835.1:p.Ala262=