Canonical Allele Identifier: CA16038728

Gene: APC

Linked Data

• dbSNP Id: rs756875223
• MyVariant Identifiers: chr5:g.112179299A>T (hg19) ; chr5:g.112843602A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843602A>T , CM000667.2:g.112843602A>T	GRCh38
NC_000005.9:g.112179299A>T , CM000667.1:g.112179299A>T	GRCh37
NC_000005.8:g.112207198A>T	NCBI36
NG_008481.4:g.156082A>T , LRG_130:g.156082A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8062A>T	ENSP00000473355.2:p.Arg2688Ter
ENST00000505350.2:c.*8014A>T	ENSP00000481752.1:n.*8014A>T
ENST00000507379.6:c.7954A>T	ENSP00000423224.2:p.Arg2652Ter
ENST00000509732.6:c.8008A>T	ENSP00000426541.2:p.Arg2670Ter
ENST00000512211.7:c.8008A>T	ENSP00000423828.3:p.Arg2670Ter
ENST00000257430.9:c.8008A>T MANE Select	ENSP00000257430.4:p.Arg2670Ter
ENST00000257430.8:c.8008A>T	ENSP00000257430.4:p.Arg2670Ter
ENST00000508376.6:c.8008A>T	ENSP00000427089.2:p.Arg2670Ter
ENST00000520401.1:c.231-13047A>T
NM_000038.5:c.8008A>T	NP_000029.2:p.Arg2670Ter
NM_001127510.2:c.8008A>T	NP_001120982.1:p.Arg2670Ter
NM_001127511.2:c.7954A>T	NP_001120983.2:p.Arg2652Ter
NM_001354895.1:c.8008A>T	NP_001341824.1:p.Arg2670Ter
NM_001354896.1:c.8062A>T	NP_001341825.1:p.Arg2688Ter
NM_001354897.1:c.8038A>T	NP_001341826.1:p.Arg2680Ter
NM_001354898.1:c.7933A>T	NP_001341827.1:p.Arg2645Ter
NM_001354899.1:c.7924A>T	NP_001341828.1:p.Arg2642Ter
NM_001354900.1:c.7885A>T	NP_001341829.1:p.Arg2629Ter
NM_001354901.1:c.7831A>T	NP_001341830.1:p.Arg2611Ter
NM_001354902.1:c.7735A>T	NP_001341831.1:p.Arg2579Ter
NM_001354903.1:c.7705A>T	NP_001341832.1:p.Arg2569Ter
NM_001354904.1:c.7630A>T	NP_001341833.1:p.Arg2544Ter
NM_001354905.1:c.7528A>T	NP_001341834.1:p.Arg2510Ter
NM_001354906.1:c.7159A>T	NP_001341835.1:p.Arg2387Ter
NM_000038.6:c.8008A>T MANE Select	NP_000029.2:p.Arg2670Ter
NM_001127510.3:c.8008A>T	NP_001120982.1:p.Arg2670Ter
NM_001127511.3:c.7954A>T	NP_001120983.2:p.Arg2652Ter
NM_001354895.2:c.8008A>T	NP_001341824.1:p.Arg2670Ter
NM_001354896.2:c.8062A>T	NP_001341825.1:p.Arg2688Ter
NM_001354897.2:c.8038A>T	NP_001341826.1:p.Arg2680Ter
NM_001354898.2:c.7933A>T	NP_001341827.1:p.Arg2645Ter
NM_001354899.2:c.7924A>T	NP_001341828.1:p.Arg2642Ter
NM_001354900.2:c.7885A>T	NP_001341829.1:p.Arg2629Ter
NM_001354901.2:c.7831A>T	NP_001341830.1:p.Arg2611Ter
NM_001354902.2:c.7735A>T	NP_001341831.1:p.Arg2579Ter
NM_001354903.2:c.7705A>T	NP_001341832.1:p.Arg2569Ter
NM_001354904.2:c.7630A>T	NP_001341833.1:p.Arg2544Ter
NM_001354905.2:c.7528A>T	NP_001341834.1:p.Arg2510Ter
NM_001354906.2:c.7159A>T	NP_001341835.1:p.Arg2387Ter