Canonical Allele Identifier: CA446208751

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112176292T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840595T>C , CM000667.2:g.112840595T>C	GRCh38
NC_000005.9:g.112176292T>C , CM000667.1:g.112176292T>C	GRCh37
NC_000005.8:g.112204191T>C	NCBI36
NG_008481.4:g.153075T>C , LRG_130:g.153075T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5055T>C	ENSP00000473355.2:p.Asn1685=
ENST00000505350.2:c.*5007T>C	ENSP00000481752.1:n.*5007T>C
ENST00000507379.6:c.4947T>C	ENSP00000423224.2:p.Asn1649=
ENST00000509732.6:c.5001T>C	ENSP00000426541.2:p.Asn1667=
ENST00000512211.7:c.5001T>C	ENSP00000423828.3:p.Asn1667=
ENST00000257430.9:c.5001T>C MANE Select	ENSP00000257430.4:p.Asn1667=
ENST00000257430.8:c.5001T>C	ENSP00000257430.4:p.Asn1667=
ENST00000508376.6:c.5001T>C	ENSP00000427089.2:p.Asn1667=
ENST00000508624.5:c.*4323T>C	ENSP00000424265.1:n.*4323T>C
ENST00000520401.1:c.230+11623T>C
NM_000038.5:c.5001T>C	NP_000029.2:p.Asn1667=
NM_001127510.2:c.5001T>C	NP_001120982.1:p.Asn1667=
NM_001127511.2:c.4947T>C	NP_001120983.2:p.Asn1649=
NM_001354895.1:c.5001T>C	NP_001341824.1:p.Asn1667=
NM_001354896.1:c.5055T>C	NP_001341825.1:p.Asn1685=
NM_001354897.1:c.5031T>C	NP_001341826.1:p.Asn1677=
NM_001354898.1:c.4926T>C	NP_001341827.1:p.Asn1642=
NM_001354899.1:c.4917T>C	NP_001341828.1:p.Asn1639=
NM_001354900.1:c.4878T>C	NP_001341829.1:p.Asn1626=
NM_001354901.1:c.4824T>C	NP_001341830.1:p.Asn1608=
NM_001354902.1:c.4728T>C	NP_001341831.1:p.Asn1576=
NM_001354903.1:c.4698T>C	NP_001341832.1:p.Asn1566=
NM_001354904.1:c.4623T>C	NP_001341833.1:p.Asn1541=
NM_001354905.1:c.4521T>C	NP_001341834.1:p.Asn1507=
NM_001354906.1:c.4152T>C	NP_001341835.1:p.Asn1384=
NM_000038.6:c.5001T>C MANE Select	NP_000029.2:p.Asn1667=
NM_001127510.3:c.5001T>C	NP_001120982.1:p.Asn1667=
NM_001127511.3:c.4947T>C	NP_001120983.2:p.Asn1649=
NM_001354895.2:c.5001T>C	NP_001341824.1:p.Asn1667=
NM_001354896.2:c.5055T>C	NP_001341825.1:p.Asn1685=
NM_001354897.2:c.5031T>C	NP_001341826.1:p.Asn1677=
NM_001354898.2:c.4926T>C	NP_001341827.1:p.Asn1642=
NM_001354899.2:c.4917T>C	NP_001341828.1:p.Asn1639=
NM_001354900.2:c.4878T>C	NP_001341829.1:p.Asn1626=
NM_001354901.2:c.4824T>C	NP_001341830.1:p.Asn1608=
NM_001354902.2:c.4728T>C	NP_001341831.1:p.Asn1576=
NM_001354903.2:c.4698T>C	NP_001341832.1:p.Asn1566=
NM_001354904.2:c.4623T>C	NP_001341833.1:p.Asn1541=
NM_001354905.2:c.4521T>C	NP_001341834.1:p.Asn1507=
NM_001354906.2:c.4152T>C	NP_001341835.1:p.Asn1384=