Canonical Allele Identifier: CA446210978

Gene: APC

Linked Data

• dbSNP Id: rs1580688611
• MyVariant Identifiers: chr5:g.112179244T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843547T>A , CM000667.2:g.112843547T>A	GRCh38
NC_000005.9:g.112179244T>A , CM000667.1:g.112179244T>A	GRCh37
NC_000005.8:g.112207143T>A	NCBI36
NG_008481.4:g.156027T>A , LRG_130:g.156027T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8007T>A	ENSP00000473355.2:p.Val2669=
ENST00000505350.2:c.*7959T>A	ENSP00000481752.1:n.*7959T>A
ENST00000507379.6:c.7899T>A	ENSP00000423224.2:p.Val2633=
ENST00000509732.6:c.7953T>A	ENSP00000426541.2:p.Val2651=
ENST00000512211.7:c.7953T>A	ENSP00000423828.3:p.Val2651=
ENST00000257430.9:c.7953T>A MANE Select	ENSP00000257430.4:p.Val2651=
ENST00000257430.8:c.7953T>A	ENSP00000257430.4:p.Val2651=
ENST00000508376.6:c.7953T>A	ENSP00000427089.2:p.Val2651=
ENST00000520401.1:c.231-13102T>A
NM_000038.5:c.7953T>A	NP_000029.2:p.Val2651=
NM_001127510.2:c.7953T>A	NP_001120982.1:p.Val2651=
NM_001127511.2:c.7899T>A	NP_001120983.2:p.Val2633=
NM_001354895.1:c.7953T>A	NP_001341824.1:p.Val2651=
NM_001354896.1:c.8007T>A	NP_001341825.1:p.Val2669=
NM_001354897.1:c.7983T>A	NP_001341826.1:p.Val2661=
NM_001354898.1:c.7878T>A	NP_001341827.1:p.Val2626=
NM_001354899.1:c.7869T>A	NP_001341828.1:p.Val2623=
NM_001354900.1:c.7830T>A	NP_001341829.1:p.Val2610=
NM_001354901.1:c.7776T>A	NP_001341830.1:p.Val2592=
NM_001354902.1:c.7680T>A	NP_001341831.1:p.Val2560=
NM_001354903.1:c.7650T>A	NP_001341832.1:p.Val2550=
NM_001354904.1:c.7575T>A	NP_001341833.1:p.Val2525=
NM_001354905.1:c.7473T>A	NP_001341834.1:p.Val2491=
NM_001354906.1:c.7104T>A	NP_001341835.1:p.Val2368=
NM_000038.6:c.7953T>A MANE Select	NP_000029.2:p.Val2651=
NM_001127510.3:c.7953T>A	NP_001120982.1:p.Val2651=
NM_001127511.3:c.7899T>A	NP_001120983.2:p.Val2633=
NM_001354895.2:c.7953T>A	NP_001341824.1:p.Val2651=
NM_001354896.2:c.8007T>A	NP_001341825.1:p.Val2669=
NM_001354897.2:c.7983T>A	NP_001341826.1:p.Val2661=
NM_001354898.2:c.7878T>A	NP_001341827.1:p.Val2626=
NM_001354899.2:c.7869T>A	NP_001341828.1:p.Val2623=
NM_001354900.2:c.7830T>A	NP_001341829.1:p.Val2610=
NM_001354901.2:c.7776T>A	NP_001341830.1:p.Val2592=
NM_001354902.2:c.7680T>A	NP_001341831.1:p.Val2560=
NM_001354903.2:c.7650T>A	NP_001341832.1:p.Val2550=
NM_001354904.2:c.7575T>A	NP_001341833.1:p.Val2525=
NM_001354905.2:c.7473T>A	NP_001341834.1:p.Val2491=
NM_001354906.2:c.7104T>A	NP_001341835.1:p.Val2368=