Canonical Allele Identifier: CA16032078

Gene: APC

Linked Data

• dbSNP Id: rs730882128
• MyVariant Identifiers: chr5:g.112176197G>C (hg19) ; chr5:g.112840500G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840500G>C , CM000667.2:g.112840500G>C	GRCh38
NC_000005.9:g.112176197G>C , CM000667.1:g.112176197G>C	GRCh37
NC_000005.8:g.112204096G>C	NCBI36
NG_008481.4:g.152980G>C , LRG_130:g.152980G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.4960G>C	ENSP00000473355.2:p.Asp1654His
ENST00000505350.2:c.*4912G>C	ENSP00000481752.1:n.*4912G>C
ENST00000507379.6:c.4852G>C	ENSP00000423224.2:p.Asp1618His
ENST00000509732.6:c.4906G>C	ENSP00000426541.2:p.Asp1636His
ENST00000512211.7:c.4906G>C	ENSP00000423828.3:p.Asp1636His
ENST00000257430.9:c.4906G>C MANE Select	ENSP00000257430.4:p.Asp1636His
ENST00000257430.8:c.4906G>C	ENSP00000257430.4:p.Asp1636His
ENST00000508376.6:c.4906G>C	ENSP00000427089.2:p.Asp1636His
ENST00000508624.5:c.*4228G>C	ENSP00000424265.1:n.*4228G>C
ENST00000520401.1:c.230+11528G>C
NM_000038.5:c.4906G>C	NP_000029.2:p.Asp1636His
NM_001127510.2:c.4906G>C	NP_001120982.1:p.Asp1636His
NM_001127511.2:c.4852G>C	NP_001120983.2:p.Asp1618His
NM_001354895.1:c.4906G>C	NP_001341824.1:p.Asp1636His
NM_001354896.1:c.4960G>C	NP_001341825.1:p.Asp1654His
NM_001354897.1:c.4936G>C	NP_001341826.1:p.Asp1646His
NM_001354898.1:c.4831G>C	NP_001341827.1:p.Asp1611His
NM_001354899.1:c.4822G>C	NP_001341828.1:p.Asp1608His
NM_001354900.1:c.4783G>C	NP_001341829.1:p.Asp1595His
NM_001354901.1:c.4729G>C	NP_001341830.1:p.Asp1577His
NM_001354902.1:c.4633G>C	NP_001341831.1:p.Asp1545His
NM_001354903.1:c.4603G>C	NP_001341832.1:p.Asp1535His
NM_001354904.1:c.4528G>C	NP_001341833.1:p.Asp1510His
NM_001354905.1:c.4426G>C	NP_001341834.1:p.Asp1476His
NM_001354906.1:c.4057G>C	NP_001341835.1:p.Asp1353His
NM_000038.6:c.4906G>C MANE Select	NP_000029.2:p.Asp1636His
NM_001127510.3:c.4906G>C	NP_001120982.1:p.Asp1636His
NM_001127511.3:c.4852G>C	NP_001120983.2:p.Asp1618His
NM_001354895.2:c.4906G>C	NP_001341824.1:p.Asp1636His
NM_001354896.2:c.4960G>C	NP_001341825.1:p.Asp1654His
NM_001354897.2:c.4936G>C	NP_001341826.1:p.Asp1646His
NM_001354898.2:c.4831G>C	NP_001341827.1:p.Asp1611His
NM_001354899.2:c.4822G>C	NP_001341828.1:p.Asp1608His
NM_001354900.2:c.4783G>C	NP_001341829.1:p.Asp1595His
NM_001354901.2:c.4729G>C	NP_001341830.1:p.Asp1577His
NM_001354902.2:c.4633G>C	NP_001341831.1:p.Asp1545His
NM_001354903.2:c.4603G>C	NP_001341832.1:p.Asp1535His
NM_001354904.2:c.4528G>C	NP_001341833.1:p.Asp1510His
NM_001354905.2:c.4426G>C	NP_001341834.1:p.Asp1476His
NM_001354906.2:c.4057G>C	NP_001341835.1:p.Asp1353His