Canonical Allele Identifier: CA445755696

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112151236T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112815539T>C , CM000667.2:g.112815539T>C	GRCh38
NC_000005.9:g.112151236T>C , CM000667.1:g.112151236T>C	GRCh37
NC_000005.8:g.112179135T>C	NCBI36
NG_008481.4:g.128019T>C , LRG_130:g.128019T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.879T>C	ENSP00000484935.2:p.Ser293=
ENST00000504915.3:c.879T>C	ENSP00000473355.2:p.Ser293=
ENST00000505084.2:n.935T>C
ENST00000505350.2:c.*885T>C	ENSP00000481752.1:n.*885T>C
ENST00000507379.6:c.825T>C	ENSP00000423224.2:p.Ser275=
ENST00000509732.6:c.879T>C	ENSP00000426541.2:p.Ser293=
ENST00000512211.7:c.879T>C	ENSP00000423828.3:p.Ser293=
ENST00000257430.9:c.879T>C MANE Select	ENSP00000257430.4:p.Ser293=
ENST00000257430.8:c.879T>C	ENSP00000257430.4:p.Ser293=
ENST00000507379.5:c.825T>C	ENSP00000423224.1:p.Ser275=
ENST00000508376.6:c.879T>C	ENSP00000427089.2:p.Ser293=
ENST00000508624.5:c.*201T>C	ENSP00000424265.1:n.*201T>C
ENST00000512211.6:c.879T>C	ENSP00000423828.2:p.Ser293=
NM_000038.5:c.879T>C	NP_000029.2:p.Ser293=
NM_001127510.2:c.879T>C	NP_001120982.1:p.Ser293=
NM_001127511.2:c.825T>C	NP_001120983.2:p.Ser275=
NM_001354895.1:c.879T>C	NP_001341824.1:p.Ser293=
NM_001354896.1:c.879T>C	NP_001341825.1:p.Ser293=
NM_001354897.1:c.909T>C	NP_001341826.1:p.Ser303=
NM_001354898.1:c.804T>C	NP_001341827.1:p.Ser268=
NM_001354899.1:c.795T>C	NP_001341828.1:p.Ser265=
NM_001354900.1:c.702T>C	NP_001341829.1:p.Ser234=
NM_001354901.1:c.702T>C	NP_001341830.1:p.Ser234=
NM_001354902.1:c.909T>C	NP_001341831.1:p.Ser303=
NM_001354903.1:c.879T>C	NP_001341832.1:p.Ser293=
NM_001354904.1:c.804T>C	NP_001341833.1:p.Ser268=
NM_001354905.1:c.702T>C	NP_001341834.1:p.Ser234=
NM_001354906.1:c.30T>C	NP_001341835.1:p.Ser10=
NM_000038.6:c.879T>C MANE Select	NP_000029.2:p.Ser293=
NM_001127510.3:c.879T>C	NP_001120982.1:p.Ser293=
NM_001127511.3:c.825T>C	NP_001120983.2:p.Ser275=
NM_001354895.2:c.879T>C	NP_001341824.1:p.Ser293=
NM_001354896.2:c.879T>C	NP_001341825.1:p.Ser293=
NM_001354897.2:c.909T>C	NP_001341826.1:p.Ser303=
NM_001354898.2:c.804T>C	NP_001341827.1:p.Ser268=
NM_001354899.2:c.795T>C	NP_001341828.1:p.Ser265=
NM_001354900.2:c.702T>C	NP_001341829.1:p.Ser234=
NM_001354901.2:c.702T>C	NP_001341830.1:p.Ser234=
NM_001354902.2:c.909T>C	NP_001341831.1:p.Ser303=
NM_001354903.2:c.879T>C	NP_001341832.1:p.Ser293=
NM_001354904.2:c.804T>C	NP_001341833.1:p.Ser268=
NM_001354905.2:c.702T>C	NP_001341834.1:p.Ser234=
NM_001354906.2:c.30T>C	NP_001341835.1:p.Ser10=