Canonical Allele Identifier: CA16025583

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112170856A>C (hg19) ; chr5:g.112835159A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835159A>C , CM000667.2:g.112835159A>C	GRCh38
NC_000005.9:g.112170856A>C , CM000667.1:g.112170856A>C	GRCh37
NC_000005.8:g.112198755A>C	NCBI36
NG_008481.4:g.147639A>C , LRG_130:g.147639A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1617A>C	ENSP00000484935.2:n.1617A>C
ENST00000504915.3:c.2006A>C	ENSP00000473355.2:p.Asp669Ala
ENST00000505350.2:c.*1958A>C	ENSP00000481752.1:n.*1958A>C
ENST00000507379.6:c.1898A>C	ENSP00000423224.2:p.Asp633Ala
ENST00000509732.6:c.1952A>C	ENSP00000426541.2:p.Asp651Ala
ENST00000512211.7:c.1952A>C	ENSP00000423828.3:p.Asp651Ala
ENST00000257430.9:c.1952A>C MANE Select	ENSP00000257430.4:p.Asp651Ala
ENST00000257430.8:c.1952A>C	ENSP00000257430.4:p.Asp651Ala
ENST00000502371.2:c.305A>C
ENST00000504915.2:c.641A>C	ENSP00000473355.1:p.Asp214Ala
ENST00000507379.5:c.1898A>C	ENSP00000423224.1:p.Asp633Ala
ENST00000508376.6:c.1952A>C	ENSP00000427089.2:p.Asp651Ala
ENST00000508624.5:c.*1274A>C	ENSP00000424265.1:n.*1274A>C
ENST00000512211.6:c.1952A>C	ENSP00000423828.2:p.Asp651Ala
ENST00000520401.1:c.230+6187A>C
NM_000038.5:c.1952A>C	NP_000029.2:p.Asp651Ala
NM_001127510.2:c.1952A>C	NP_001120982.1:p.Asp651Ala
NM_001127511.2:c.1898A>C	NP_001120983.2:p.Asp633Ala
NM_001354895.1:c.1952A>C	NP_001341824.1:p.Asp651Ala
NM_001354896.1:c.2006A>C	NP_001341825.1:p.Asp669Ala
NM_001354897.1:c.1982A>C	NP_001341826.1:p.Asp661Ala
NM_001354898.1:c.1877A>C	NP_001341827.1:p.Asp626Ala
NM_001354899.1:c.1868A>C	NP_001341828.1:p.Asp623Ala
NM_001354900.1:c.1829A>C	NP_001341829.1:p.Asp610Ala
NM_001354901.1:c.1775A>C	NP_001341830.1:p.Asp592Ala
NM_001354902.1:c.1679A>C	NP_001341831.1:p.Asp560Ala
NM_001354903.1:c.1649A>C	NP_001341832.1:p.Asp550Ala
NM_001354904.1:c.1574A>C	NP_001341833.1:p.Asp525Ala
NM_001354905.1:c.1472A>C	NP_001341834.1:p.Asp491Ala
NM_001354906.1:c.1103A>C	NP_001341835.1:p.Asp368Ala
NM_000038.6:c.1952A>C MANE Select	NP_000029.2:p.Asp651Ala
NM_001127510.3:c.1952A>C	NP_001120982.1:p.Asp651Ala
NM_001127511.3:c.1898A>C	NP_001120983.2:p.Asp633Ala
NM_001354895.2:c.1952A>C	NP_001341824.1:p.Asp651Ala
NM_001354896.2:c.2006A>C	NP_001341825.1:p.Asp669Ala
NM_001354897.2:c.1982A>C	NP_001341826.1:p.Asp661Ala
NM_001354898.2:c.1877A>C	NP_001341827.1:p.Asp626Ala
NM_001354899.2:c.1868A>C	NP_001341828.1:p.Asp623Ala
NM_001354900.2:c.1829A>C	NP_001341829.1:p.Asp610Ala
NM_001354901.2:c.1775A>C	NP_001341830.1:p.Asp592Ala
NM_001354902.2:c.1679A>C	NP_001341831.1:p.Asp560Ala
NM_001354903.2:c.1649A>C	NP_001341832.1:p.Asp550Ala
NM_001354904.2:c.1574A>C	NP_001341833.1:p.Asp525Ala
NM_001354905.2:c.1472A>C	NP_001341834.1:p.Asp491Ala
NM_001354906.2:c.1103A>C	NP_001341835.1:p.Asp368Ala