Canonical Allele Identifier: CA16038640

Gene: APC

Linked Data

• dbSNP Id: rs2149997171
• MyVariant Identifiers: chr5:g.112179261T>A (hg19) ; chr5:g.112843564T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843564T>A , CM000667.2:g.112843564T>A	GRCh38
NC_000005.9:g.112179261T>A , CM000667.1:g.112179261T>A	GRCh37
NC_000005.8:g.112207160T>A	NCBI36
NG_008481.4:g.156044T>A , LRG_130:g.156044T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8024T>A	ENSP00000473355.2:p.Val2675Asp
ENST00000505350.2:c.*7976T>A	ENSP00000481752.1:n.*7976T>A
ENST00000507379.6:c.7916T>A	ENSP00000423224.2:p.Val2639Asp
ENST00000509732.6:c.7970T>A	ENSP00000426541.2:p.Val2657Asp
ENST00000512211.7:c.7970T>A	ENSP00000423828.3:p.Val2657Asp
ENST00000257430.9:c.7970T>A MANE Select	ENSP00000257430.4:p.Val2657Asp
ENST00000257430.8:c.7970T>A	ENSP00000257430.4:p.Val2657Asp
ENST00000508376.6:c.7970T>A	ENSP00000427089.2:p.Val2657Asp
ENST00000520401.1:c.231-13085T>A
NM_000038.5:c.7970T>A	NP_000029.2:p.Val2657Asp
NM_001127510.2:c.7970T>A	NP_001120982.1:p.Val2657Asp
NM_001127511.2:c.7916T>A	NP_001120983.2:p.Val2639Asp
NM_001354895.1:c.7970T>A	NP_001341824.1:p.Val2657Asp
NM_001354896.1:c.8024T>A	NP_001341825.1:p.Val2675Asp
NM_001354897.1:c.8000T>A	NP_001341826.1:p.Val2667Asp
NM_001354898.1:c.7895T>A	NP_001341827.1:p.Val2632Asp
NM_001354899.1:c.7886T>A	NP_001341828.1:p.Val2629Asp
NM_001354900.1:c.7847T>A	NP_001341829.1:p.Val2616Asp
NM_001354901.1:c.7793T>A	NP_001341830.1:p.Val2598Asp
NM_001354902.1:c.7697T>A	NP_001341831.1:p.Val2566Asp
NM_001354903.1:c.7667T>A	NP_001341832.1:p.Val2556Asp
NM_001354904.1:c.7592T>A	NP_001341833.1:p.Val2531Asp
NM_001354905.1:c.7490T>A	NP_001341834.1:p.Val2497Asp
NM_001354906.1:c.7121T>A	NP_001341835.1:p.Val2374Asp
NM_000038.6:c.7970T>A MANE Select	NP_000029.2:p.Val2657Asp
NM_001127510.3:c.7970T>A	NP_001120982.1:p.Val2657Asp
NM_001127511.3:c.7916T>A	NP_001120983.2:p.Val2639Asp
NM_001354895.2:c.7970T>A	NP_001341824.1:p.Val2657Asp
NM_001354896.2:c.8024T>A	NP_001341825.1:p.Val2675Asp
NM_001354897.2:c.8000T>A	NP_001341826.1:p.Val2667Asp
NM_001354898.2:c.7895T>A	NP_001341827.1:p.Val2632Asp
NM_001354899.2:c.7886T>A	NP_001341828.1:p.Val2629Asp
NM_001354900.2:c.7847T>A	NP_001341829.1:p.Val2616Asp
NM_001354901.2:c.7793T>A	NP_001341830.1:p.Val2598Asp
NM_001354902.2:c.7697T>A	NP_001341831.1:p.Val2566Asp
NM_001354903.2:c.7667T>A	NP_001341832.1:p.Val2556Asp
NM_001354904.2:c.7592T>A	NP_001341833.1:p.Val2531Asp
NM_001354905.2:c.7490T>A	NP_001341834.1:p.Val2497Asp
NM_001354906.2:c.7121T>A	NP_001341835.1:p.Val2374Asp