Canonical Allele Identifier: CA446208109

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112176187T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840490T>C , CM000667.2:g.112840490T>C	GRCh38
NC_000005.9:g.112176187T>C , CM000667.1:g.112176187T>C	GRCh37
NC_000005.8:g.112204086T>C	NCBI36
NG_008481.4:g.152970T>C , LRG_130:g.152970T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4950T>C	ENSP00000473355.2:p.Phe1650=
ENST00000505350.2:c.*4902T>C	ENSP00000481752.1:n.*4902T>C
ENST00000507379.6:c.4842T>C	ENSP00000423224.2:p.Phe1614=
ENST00000509732.6:c.4896T>C	ENSP00000426541.2:p.Phe1632=
ENST00000512211.7:c.4896T>C	ENSP00000423828.3:p.Phe1632=
ENST00000257430.9:c.4896T>C MANE Select	ENSP00000257430.4:p.Phe1632=
ENST00000257430.8:c.4896T>C	ENSP00000257430.4:p.Phe1632=
ENST00000508376.6:c.4896T>C	ENSP00000427089.2:p.Phe1632=
ENST00000508624.5:c.*4218T>C	ENSP00000424265.1:n.*4218T>C
ENST00000520401.1:c.230+11518T>C
NM_000038.5:c.4896T>C	NP_000029.2:p.Phe1632=
NM_001127510.2:c.4896T>C	NP_001120982.1:p.Phe1632=
NM_001127511.2:c.4842T>C	NP_001120983.2:p.Phe1614=
NM_001354895.1:c.4896T>C	NP_001341824.1:p.Phe1632=
NM_001354896.1:c.4950T>C	NP_001341825.1:p.Phe1650=
NM_001354897.1:c.4926T>C	NP_001341826.1:p.Phe1642=
NM_001354898.1:c.4821T>C	NP_001341827.1:p.Phe1607=
NM_001354899.1:c.4812T>C	NP_001341828.1:p.Phe1604=
NM_001354900.1:c.4773T>C	NP_001341829.1:p.Phe1591=
NM_001354901.1:c.4719T>C	NP_001341830.1:p.Phe1573=
NM_001354902.1:c.4623T>C	NP_001341831.1:p.Phe1541=
NM_001354903.1:c.4593T>C	NP_001341832.1:p.Phe1531=
NM_001354904.1:c.4518T>C	NP_001341833.1:p.Phe1506=
NM_001354905.1:c.4416T>C	NP_001341834.1:p.Phe1472=
NM_001354906.1:c.4047T>C	NP_001341835.1:p.Phe1349=
NM_000038.6:c.4896T>C MANE Select	NP_000029.2:p.Phe1632=
NM_001127510.3:c.4896T>C	NP_001120982.1:p.Phe1632=
NM_001127511.3:c.4842T>C	NP_001120983.2:p.Phe1614=
NM_001354895.2:c.4896T>C	NP_001341824.1:p.Phe1632=
NM_001354896.2:c.4950T>C	NP_001341825.1:p.Phe1650=
NM_001354897.2:c.4926T>C	NP_001341826.1:p.Phe1642=
NM_001354898.2:c.4821T>C	NP_001341827.1:p.Phe1607=
NM_001354899.2:c.4812T>C	NP_001341828.1:p.Phe1604=
NM_001354900.2:c.4773T>C	NP_001341829.1:p.Phe1591=
NM_001354901.2:c.4719T>C	NP_001341830.1:p.Phe1573=
NM_001354902.2:c.4623T>C	NP_001341831.1:p.Phe1541=
NM_001354903.2:c.4593T>C	NP_001341832.1:p.Phe1531=
NM_001354904.2:c.4518T>C	NP_001341833.1:p.Phe1506=
NM_001354905.2:c.4416T>C	NP_001341834.1:p.Phe1472=
NM_001354906.2:c.4047T>C	NP_001341835.1:p.Phe1349=