Canonical Allele Identifier: CA16039020

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112179438T>C (hg19) ; chr5:g.112843741T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843741T>C , CM000667.2:g.112843741T>C	GRCh38
NC_000005.9:g.112179438T>C , CM000667.1:g.112179438T>C	GRCh37
NC_000005.8:g.112207337T>C	NCBI36
NG_008481.4:g.156221T>C , LRG_130:g.156221T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8201T>C	ENSP00000473355.2:p.Val2734Ala
ENST00000505350.2:c.*8153T>C	ENSP00000481752.1:n.*8153T>C
ENST00000507379.6:c.8093T>C	ENSP00000423224.2:p.Val2698Ala
ENST00000509732.6:c.8147T>C	ENSP00000426541.2:p.Val2716Ala
ENST00000512211.7:c.8147T>C	ENSP00000423828.3:p.Val2716Ala
ENST00000257430.9:c.8147T>C MANE Select	ENSP00000257430.4:p.Val2716Ala
ENST00000257430.8:c.8147T>C	ENSP00000257430.4:p.Val2716Ala
ENST00000508376.6:c.8147T>C	ENSP00000427089.2:p.Val2716Ala
ENST00000520401.1:c.231-12908T>C
NM_000038.5:c.8147T>C	NP_000029.2:p.Val2716Ala
NM_001127510.2:c.8147T>C	NP_001120982.1:p.Val2716Ala
NM_001127511.2:c.8093T>C	NP_001120983.2:p.Val2698Ala
NM_001354895.1:c.8147T>C	NP_001341824.1:p.Val2716Ala
NM_001354896.1:c.8201T>C	NP_001341825.1:p.Val2734Ala
NM_001354897.1:c.8177T>C	NP_001341826.1:p.Val2726Ala
NM_001354898.1:c.8072T>C	NP_001341827.1:p.Val2691Ala
NM_001354899.1:c.8063T>C	NP_001341828.1:p.Val2688Ala
NM_001354900.1:c.8024T>C	NP_001341829.1:p.Val2675Ala
NM_001354901.1:c.7970T>C	NP_001341830.1:p.Val2657Ala
NM_001354902.1:c.7874T>C	NP_001341831.1:p.Val2625Ala
NM_001354903.1:c.7844T>C	NP_001341832.1:p.Val2615Ala
NM_001354904.1:c.7769T>C	NP_001341833.1:p.Val2590Ala
NM_001354905.1:c.7667T>C	NP_001341834.1:p.Val2556Ala
NM_001354906.1:c.7298T>C	NP_001341835.1:p.Val2433Ala
NM_000038.6:c.8147T>C MANE Select	NP_000029.2:p.Val2716Ala
NM_001127510.3:c.8147T>C	NP_001120982.1:p.Val2716Ala
NM_001127511.3:c.8093T>C	NP_001120983.2:p.Val2698Ala
NM_001354895.2:c.8147T>C	NP_001341824.1:p.Val2716Ala
NM_001354896.2:c.8201T>C	NP_001341825.1:p.Val2734Ala
NM_001354897.2:c.8177T>C	NP_001341826.1:p.Val2726Ala
NM_001354898.2:c.8072T>C	NP_001341827.1:p.Val2691Ala
NM_001354899.2:c.8063T>C	NP_001341828.1:p.Val2688Ala
NM_001354900.2:c.8024T>C	NP_001341829.1:p.Val2675Ala
NM_001354901.2:c.7970T>C	NP_001341830.1:p.Val2657Ala
NM_001354902.2:c.7874T>C	NP_001341831.1:p.Val2625Ala
NM_001354903.2:c.7844T>C	NP_001341832.1:p.Val2615Ala
NM_001354904.2:c.7769T>C	NP_001341833.1:p.Val2590Ala
NM_001354905.2:c.7667T>C	NP_001341834.1:p.Val2556Ala
NM_001354906.2:c.7298T>C	NP_001341835.1:p.Val2433Ala