Canonical Allele Identifier: CA16032353

Gene: APC

Linked Data

• dbSNP Id: rs2149930484
• MyVariant Identifiers: chr5:g.112176331G>C (hg19) ; chr5:g.112840634G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840634G>C , CM000667.2:g.112840634G>C	GRCh38
NC_000005.9:g.112176331G>C , CM000667.1:g.112176331G>C	GRCh37
NC_000005.8:g.112204230G>C	NCBI36
NG_008481.4:g.153114G>C , LRG_130:g.153114G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5094G>C	ENSP00000473355.2:p.Gln1698His
ENST00000505350.2:c.*5046G>C	ENSP00000481752.1:n.*5046G>C
ENST00000507379.6:c.4986G>C	ENSP00000423224.2:p.Gln1662His
ENST00000509732.6:c.5040G>C	ENSP00000426541.2:p.Gln1680His
ENST00000512211.7:c.5040G>C	ENSP00000423828.3:p.Gln1680His
ENST00000257430.9:c.5040G>C MANE Select	ENSP00000257430.4:p.Gln1680His
ENST00000257430.8:c.5040G>C	ENSP00000257430.4:p.Gln1680His
ENST00000508376.6:c.5040G>C	ENSP00000427089.2:p.Gln1680His
ENST00000508624.5:c.*4362G>C	ENSP00000424265.1:n.*4362G>C
ENST00000520401.1:c.230+11662G>C
NM_000038.5:c.5040G>C	NP_000029.2:p.Gln1680His
NM_001127510.2:c.5040G>C	NP_001120982.1:p.Gln1680His
NM_001127511.2:c.4986G>C	NP_001120983.2:p.Gln1662His
NM_001354895.1:c.5040G>C	NP_001341824.1:p.Gln1680His
NM_001354896.1:c.5094G>C	NP_001341825.1:p.Gln1698His
NM_001354897.1:c.5070G>C	NP_001341826.1:p.Gln1690His
NM_001354898.1:c.4965G>C	NP_001341827.1:p.Gln1655His
NM_001354899.1:c.4956G>C	NP_001341828.1:p.Gln1652His
NM_001354900.1:c.4917G>C	NP_001341829.1:p.Gln1639His
NM_001354901.1:c.4863G>C	NP_001341830.1:p.Gln1621His
NM_001354902.1:c.4767G>C	NP_001341831.1:p.Gln1589His
NM_001354903.1:c.4737G>C	NP_001341832.1:p.Gln1579His
NM_001354904.1:c.4662G>C	NP_001341833.1:p.Gln1554His
NM_001354905.1:c.4560G>C	NP_001341834.1:p.Gln1520His
NM_001354906.1:c.4191G>C	NP_001341835.1:p.Gln1397His
NM_000038.6:c.5040G>C MANE Select	NP_000029.2:p.Gln1680His
NM_001127510.3:c.5040G>C	NP_001120982.1:p.Gln1680His
NM_001127511.3:c.4986G>C	NP_001120983.2:p.Gln1662His
NM_001354895.2:c.5040G>C	NP_001341824.1:p.Gln1680His
NM_001354896.2:c.5094G>C	NP_001341825.1:p.Gln1698His
NM_001354897.2:c.5070G>C	NP_001341826.1:p.Gln1690His
NM_001354898.2:c.4965G>C	NP_001341827.1:p.Gln1655His
NM_001354899.2:c.4956G>C	NP_001341828.1:p.Gln1652His
NM_001354900.2:c.4917G>C	NP_001341829.1:p.Gln1639His
NM_001354901.2:c.4863G>C	NP_001341830.1:p.Gln1621His
NM_001354902.2:c.4767G>C	NP_001341831.1:p.Gln1589His
NM_001354903.2:c.4737G>C	NP_001341832.1:p.Gln1579His
NM_001354904.2:c.4662G>C	NP_001341833.1:p.Gln1554His
NM_001354905.2:c.4560G>C	NP_001341834.1:p.Gln1520His
NM_001354906.2:c.4191G>C	NP_001341835.1:p.Gln1397His