Canonical Allele Identifier: CA446206604

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112175875T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840178T>C , CM000667.2:g.112840178T>C	GRCh38
NC_000005.9:g.112175875T>C , CM000667.1:g.112175875T>C	GRCh37
NC_000005.8:g.112203774T>C	NCBI36
NG_008481.4:g.152658T>C , LRG_130:g.152658T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4638T>C	ENSP00000473355.2:p.Val1546=
ENST00000505350.2:c.*4590T>C	ENSP00000481752.1:n.*4590T>C
ENST00000507379.6:c.4530T>C	ENSP00000423224.2:p.Val1510=
ENST00000509732.6:c.4584T>C	ENSP00000426541.2:p.Val1528=
ENST00000512211.7:c.4584T>C	ENSP00000423828.3:p.Val1528=
ENST00000257430.9:c.4584T>C MANE Select	ENSP00000257430.4:p.Val1528=
ENST00000257430.8:c.4584T>C	ENSP00000257430.4:p.Val1528=
ENST00000508376.6:c.4584T>C	ENSP00000427089.2:p.Val1528=
ENST00000508624.5:c.*3906T>C	ENSP00000424265.1:n.*3906T>C
ENST00000520401.1:c.230+11206T>C
NM_000038.5:c.4584T>C	NP_000029.2:p.Val1528=
NM_001127510.2:c.4584T>C	NP_001120982.1:p.Val1528=
NM_001127511.2:c.4530T>C	NP_001120983.2:p.Val1510=
NM_001354895.1:c.4584T>C	NP_001341824.1:p.Val1528=
NM_001354896.1:c.4638T>C	NP_001341825.1:p.Val1546=
NM_001354897.1:c.4614T>C	NP_001341826.1:p.Val1538=
NM_001354898.1:c.4509T>C	NP_001341827.1:p.Val1503=
NM_001354899.1:c.4500T>C	NP_001341828.1:p.Val1500=
NM_001354900.1:c.4461T>C	NP_001341829.1:p.Val1487=
NM_001354901.1:c.4407T>C	NP_001341830.1:p.Val1469=
NM_001354902.1:c.4311T>C	NP_001341831.1:p.Val1437=
NM_001354903.1:c.4281T>C	NP_001341832.1:p.Val1427=
NM_001354904.1:c.4206T>C	NP_001341833.1:p.Val1402=
NM_001354905.1:c.4104T>C	NP_001341834.1:p.Val1368=
NM_001354906.1:c.3735T>C	NP_001341835.1:p.Val1245=
NM_000038.6:c.4584T>C MANE Select	NP_000029.2:p.Val1528=
NM_001127510.3:c.4584T>C	NP_001120982.1:p.Val1528=
NM_001127511.3:c.4530T>C	NP_001120983.2:p.Val1510=
NM_001354895.2:c.4584T>C	NP_001341824.1:p.Val1528=
NM_001354896.2:c.4638T>C	NP_001341825.1:p.Val1546=
NM_001354897.2:c.4614T>C	NP_001341826.1:p.Val1538=
NM_001354898.2:c.4509T>C	NP_001341827.1:p.Val1503=
NM_001354899.2:c.4500T>C	NP_001341828.1:p.Val1500=
NM_001354900.2:c.4461T>C	NP_001341829.1:p.Val1487=
NM_001354901.2:c.4407T>C	NP_001341830.1:p.Val1469=
NM_001354902.2:c.4311T>C	NP_001341831.1:p.Val1437=
NM_001354903.2:c.4281T>C	NP_001341832.1:p.Val1427=
NM_001354904.2:c.4206T>C	NP_001341833.1:p.Val1402=
NM_001354905.2:c.4104T>C	NP_001341834.1:p.Val1368=
NM_001354906.2:c.3735T>C	NP_001341835.1:p.Val1245=