Canonical Allele Identifier: CA16038746

Gene: APC

Linked Data

• dbSNP Id: rs539168162
• MyVariant Identifiers: chr5:g.112179309G>C (hg19) ; chr5:g.112843612G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843612G>C , CM000667.2:g.112843612G>C	GRCh38
NC_000005.9:g.112179309G>C , CM000667.1:g.112179309G>C	GRCh37
NC_000005.8:g.112207208G>C	NCBI36
NG_008481.4:g.156092G>C , LRG_130:g.156092G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8072G>C	ENSP00000473355.2:p.Arg2691Thr
ENST00000505350.2:c.*8024G>C	ENSP00000481752.1:n.*8024G>C
ENST00000507379.6:c.7964G>C	ENSP00000423224.2:p.Arg2655Thr
ENST00000509732.6:c.8018G>C	ENSP00000426541.2:p.Arg2673Thr
ENST00000512211.7:c.8018G>C	ENSP00000423828.3:p.Arg2673Thr
ENST00000257430.9:c.8018G>C MANE Select	ENSP00000257430.4:p.Arg2673Thr
ENST00000257430.8:c.8018G>C	ENSP00000257430.4:p.Arg2673Thr
ENST00000508376.6:c.8018G>C	ENSP00000427089.2:p.Arg2673Thr
ENST00000520401.1:c.231-13037G>C
NM_000038.5:c.8018G>C	NP_000029.2:p.Arg2673Thr
NM_001127510.2:c.8018G>C	NP_001120982.1:p.Arg2673Thr
NM_001127511.2:c.7964G>C	NP_001120983.2:p.Arg2655Thr
NM_001354895.1:c.8018G>C	NP_001341824.1:p.Arg2673Thr
NM_001354896.1:c.8072G>C	NP_001341825.1:p.Arg2691Thr
NM_001354897.1:c.8048G>C	NP_001341826.1:p.Arg2683Thr
NM_001354898.1:c.7943G>C	NP_001341827.1:p.Arg2648Thr
NM_001354899.1:c.7934G>C	NP_001341828.1:p.Arg2645Thr
NM_001354900.1:c.7895G>C	NP_001341829.1:p.Arg2632Thr
NM_001354901.1:c.7841G>C	NP_001341830.1:p.Arg2614Thr
NM_001354902.1:c.7745G>C	NP_001341831.1:p.Arg2582Thr
NM_001354903.1:c.7715G>C	NP_001341832.1:p.Arg2572Thr
NM_001354904.1:c.7640G>C	NP_001341833.1:p.Arg2547Thr
NM_001354905.1:c.7538G>C	NP_001341834.1:p.Arg2513Thr
NM_001354906.1:c.7169G>C	NP_001341835.1:p.Arg2390Thr
NM_000038.6:c.8018G>C MANE Select	NP_000029.2:p.Arg2673Thr
NM_001127510.3:c.8018G>C	NP_001120982.1:p.Arg2673Thr
NM_001127511.3:c.7964G>C	NP_001120983.2:p.Arg2655Thr
NM_001354895.2:c.8018G>C	NP_001341824.1:p.Arg2673Thr
NM_001354896.2:c.8072G>C	NP_001341825.1:p.Arg2691Thr
NM_001354897.2:c.8048G>C	NP_001341826.1:p.Arg2683Thr
NM_001354898.2:c.7943G>C	NP_001341827.1:p.Arg2648Thr
NM_001354899.2:c.7934G>C	NP_001341828.1:p.Arg2645Thr
NM_001354900.2:c.7895G>C	NP_001341829.1:p.Arg2632Thr
NM_001354901.2:c.7841G>C	NP_001341830.1:p.Arg2614Thr
NM_001354902.2:c.7745G>C	NP_001341831.1:p.Arg2582Thr
NM_001354903.2:c.7715G>C	NP_001341832.1:p.Arg2572Thr
NM_001354904.2:c.7640G>C	NP_001341833.1:p.Arg2547Thr
NM_001354905.2:c.7538G>C	NP_001341834.1:p.Arg2513Thr
NM_001354906.2:c.7169G>C	NP_001341835.1:p.Arg2390Thr