Canonical Allele Identifier: CA445758838

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112170695A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112834998A>C , CM000667.2:g.112834998A>C	GRCh38
NC_000005.9:g.112170695A>C , CM000667.1:g.112170695A>C	GRCh37
NC_000005.8:g.112198594A>C	NCBI36
NG_008481.4:g.147478A>C , LRG_130:g.147478A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1456A>C	ENSP00000484935.2:p.Thr486Pro
ENST00000504915.3:c.1845A>C	ENSP00000473355.2:p.Ala615=
ENST00000505350.2:c.*1797A>C	ENSP00000481752.1:n.*1797A>C
ENST00000507379.6:c.1737A>C	ENSP00000423224.2:p.Ala579=
ENST00000509732.6:c.1791A>C	ENSP00000426541.2:p.Ala597=
ENST00000512211.7:c.1791A>C	ENSP00000423828.3:p.Ala597=
ENST00000257430.9:c.1791A>C MANE Select	ENSP00000257430.4:p.Ala597=
ENST00000257430.8:c.1791A>C	ENSP00000257430.4:p.Ala597=
ENST00000502371.2:c.144A>C
ENST00000504915.2:c.480A>C	ENSP00000473355.1:p.Ala160=
ENST00000507379.5:c.1737A>C	ENSP00000423224.1:p.Ala579=
ENST00000508376.6:c.1791A>C	ENSP00000427089.2:p.Ala597=
ENST00000508624.5:c.*1113A>C	ENSP00000424265.1:n.*1113A>C
ENST00000512211.6:c.1791A>C	ENSP00000423828.2:p.Ala597=
ENST00000520401.1:c.230+6026A>C
NM_000038.5:c.1791A>C	NP_000029.2:p.Ala597=
NM_001127510.2:c.1791A>C	NP_001120982.1:p.Ala597=
NM_001127511.2:c.1737A>C	NP_001120983.2:p.Ala579=
NM_001354895.1:c.1791A>C	NP_001341824.1:p.Ala597=
NM_001354896.1:c.1845A>C	NP_001341825.1:p.Ala615=
NM_001354897.1:c.1821A>C	NP_001341826.1:p.Ala607=
NM_001354898.1:c.1716A>C	NP_001341827.1:p.Ala572=
NM_001354899.1:c.1707A>C	NP_001341828.1:p.Ala569=
NM_001354900.1:c.1668A>C	NP_001341829.1:p.Ala556=
NM_001354901.1:c.1614A>C	NP_001341830.1:p.Ala538=
NM_001354902.1:c.1518A>C	NP_001341831.1:p.Ala506=
NM_001354903.1:c.1488A>C	NP_001341832.1:p.Ala496=
NM_001354904.1:c.1413A>C	NP_001341833.1:p.Ala471=
NM_001354905.1:c.1311A>C	NP_001341834.1:p.Ala437=
NM_001354906.1:c.942A>C	NP_001341835.1:p.Ala314=
NM_000038.6:c.1791A>C MANE Select	NP_000029.2:p.Ala597=
NM_001127510.3:c.1791A>C	NP_001120982.1:p.Ala597=
NM_001127511.3:c.1737A>C	NP_001120983.2:p.Ala579=
NM_001354895.2:c.1791A>C	NP_001341824.1:p.Ala597=
NM_001354896.2:c.1845A>C	NP_001341825.1:p.Ala615=
NM_001354897.2:c.1821A>C	NP_001341826.1:p.Ala607=
NM_001354898.2:c.1716A>C	NP_001341827.1:p.Ala572=
NM_001354899.2:c.1707A>C	NP_001341828.1:p.Ala569=
NM_001354900.2:c.1668A>C	NP_001341829.1:p.Ala556=
NM_001354901.2:c.1614A>C	NP_001341830.1:p.Ala538=
NM_001354902.2:c.1518A>C	NP_001341831.1:p.Ala506=
NM_001354903.2:c.1488A>C	NP_001341832.1:p.Ala496=
NM_001354904.2:c.1413A>C	NP_001341833.1:p.Ala471=
NM_001354905.2:c.1311A>C	NP_001341834.1:p.Ala437=
NM_001354906.2:c.942A>C	NP_001341835.1:p.Ala314=