Canonical Allele Identifier: CA16029529

Gene: APC

Linked Data

• ClinVar Variation Id: 926764
• ClinVar RCV Id: RCV001189574
• dbSNP Id: rs1765505976
• MyVariant Identifiers: chr5:g.112175026G>C (hg19) ; chr5:g.112839329G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839329G>C , CM000667.2:g.112839329G>C	GRCh38
NC_000005.9:g.112175026G>C , CM000667.1:g.112175026G>C	GRCh37
NC_000005.8:g.112202925G>C	NCBI36
NG_008481.4:g.151809G>C , LRG_130:g.151809G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3400G>C	ENSP00000484935.2:n.3400G>C
ENST00000504915.3:c.3789G>C	ENSP00000473355.2:p.Lys1263Asn
ENST00000505350.2:c.*3741G>C	ENSP00000481752.1:n.*3741G>C
ENST00000507379.6:c.3681G>C	ENSP00000423224.2:p.Lys1227Asn
ENST00000509732.6:c.3735G>C	ENSP00000426541.2:p.Lys1245Asn
ENST00000512211.7:c.3735G>C	ENSP00000423828.3:p.Lys1245Asn
ENST00000257430.9:c.3735G>C MANE Select	ENSP00000257430.4:p.Lys1245Asn
ENST00000257430.8:c.3735G>C	ENSP00000257430.4:p.Lys1245Asn
ENST00000502371.2:c.2088G>C
ENST00000508376.6:c.3735G>C	ENSP00000427089.2:p.Lys1245Asn
ENST00000508624.5:c.*3057G>C	ENSP00000424265.1:n.*3057G>C
ENST00000512211.6:c.3735G>C	ENSP00000423828.2:p.Lys1245Asn
ENST00000520401.1:c.230+10357G>C
NM_000038.5:c.3735G>C	NP_000029.2:p.Lys1245Asn
NM_001127510.2:c.3735G>C	NP_001120982.1:p.Lys1245Asn
NM_001127511.2:c.3681G>C	NP_001120983.2:p.Lys1227Asn
NM_001354895.1:c.3735G>C	NP_001341824.1:p.Lys1245Asn
NM_001354896.1:c.3789G>C	NP_001341825.1:p.Lys1263Asn
NM_001354897.1:c.3765G>C	NP_001341826.1:p.Lys1255Asn
NM_001354898.1:c.3660G>C	NP_001341827.1:p.Lys1220Asn
NM_001354899.1:c.3651G>C	NP_001341828.1:p.Lys1217Asn
NM_001354900.1:c.3612G>C	NP_001341829.1:p.Lys1204Asn
NM_001354901.1:c.3558G>C	NP_001341830.1:p.Lys1186Asn
NM_001354902.1:c.3462G>C	NP_001341831.1:p.Lys1154Asn
NM_001354903.1:c.3432G>C	NP_001341832.1:p.Lys1144Asn
NM_001354904.1:c.3357G>C	NP_001341833.1:p.Lys1119Asn
NM_001354905.1:c.3255G>C	NP_001341834.1:p.Lys1085Asn
NM_001354906.1:c.2886G>C	NP_001341835.1:p.Lys962Asn
NM_000038.6:c.3735G>C MANE Select	NP_000029.2:p.Lys1245Asn
NM_001127510.3:c.3735G>C	NP_001120982.1:p.Lys1245Asn
NM_001127511.3:c.3681G>C	NP_001120983.2:p.Lys1227Asn
NM_001354895.2:c.3735G>C	NP_001341824.1:p.Lys1245Asn
NM_001354896.2:c.3789G>C	NP_001341825.1:p.Lys1263Asn
NM_001354897.2:c.3765G>C	NP_001341826.1:p.Lys1255Asn
NM_001354898.2:c.3660G>C	NP_001341827.1:p.Lys1220Asn
NM_001354899.2:c.3651G>C	NP_001341828.1:p.Lys1217Asn
NM_001354900.2:c.3612G>C	NP_001341829.1:p.Lys1204Asn
NM_001354901.2:c.3558G>C	NP_001341830.1:p.Lys1186Asn
NM_001354902.2:c.3462G>C	NP_001341831.1:p.Lys1154Asn
NM_001354903.2:c.3432G>C	NP_001341832.1:p.Lys1144Asn
NM_001354904.2:c.3357G>C	NP_001341833.1:p.Lys1119Asn
NM_001354905.2:c.3255G>C	NP_001341834.1:p.Lys1085Asn
NM_001354906.2:c.2886G>C	NP_001341835.1:p.Lys962Asn