Canonical Allele Identifier: CA16025481

Gene: APC

Linked Data

• dbSNP Id: rs1554083205
• MyVariant Identifiers: chr5:g.112170807G>C (hg19) ; chr5:g.112835110G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835110G>C , CM000667.2:g.112835110G>C	GRCh38
NC_000005.9:g.112170807G>C , CM000667.1:g.112170807G>C	GRCh37
NC_000005.8:g.112198706G>C	NCBI36
NG_008481.4:g.147590G>C , LRG_130:g.147590G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1568G>C	ENSP00000484935.2:n.1568G>C
ENST00000504915.3:c.1957G>C	ENSP00000473355.2:p.Gly653Arg
ENST00000505350.2:c.*1909G>C	ENSP00000481752.1:n.*1909G>C
ENST00000507379.6:c.1849G>C	ENSP00000423224.2:p.Gly617Arg
ENST00000509732.6:c.1903G>C	ENSP00000426541.2:p.Gly635Arg
ENST00000512211.7:c.1903G>C	ENSP00000423828.3:p.Gly635Arg
ENST00000257430.9:c.1903G>C MANE Select	ENSP00000257430.4:p.Gly635Arg
ENST00000257430.8:c.1903G>C	ENSP00000257430.4:p.Gly635Arg
ENST00000502371.2:c.256G>C
ENST00000504915.2:c.592G>C	ENSP00000473355.1:p.Gly198Arg
ENST00000507379.5:c.1849G>C	ENSP00000423224.1:p.Gly617Arg
ENST00000508376.6:c.1903G>C	ENSP00000427089.2:p.Gly635Arg
ENST00000508624.5:c.*1225G>C	ENSP00000424265.1:n.*1225G>C
ENST00000512211.6:c.1903G>C	ENSP00000423828.2:p.Gly635Arg
ENST00000520401.1:c.230+6138G>C
NM_000038.5:c.1903G>C	NP_000029.2:p.Gly635Arg
NM_001127510.2:c.1903G>C	NP_001120982.1:p.Gly635Arg
NM_001127511.2:c.1849G>C	NP_001120983.2:p.Gly617Arg
NM_001354895.1:c.1903G>C	NP_001341824.1:p.Gly635Arg
NM_001354896.1:c.1957G>C	NP_001341825.1:p.Gly653Arg
NM_001354897.1:c.1933G>C	NP_001341826.1:p.Gly645Arg
NM_001354898.1:c.1828G>C	NP_001341827.1:p.Gly610Arg
NM_001354899.1:c.1819G>C	NP_001341828.1:p.Gly607Arg
NM_001354900.1:c.1780G>C	NP_001341829.1:p.Gly594Arg
NM_001354901.1:c.1726G>C	NP_001341830.1:p.Gly576Arg
NM_001354902.1:c.1630G>C	NP_001341831.1:p.Gly544Arg
NM_001354903.1:c.1600G>C	NP_001341832.1:p.Gly534Arg
NM_001354904.1:c.1525G>C	NP_001341833.1:p.Gly509Arg
NM_001354905.1:c.1423G>C	NP_001341834.1:p.Gly475Arg
NM_001354906.1:c.1054G>C	NP_001341835.1:p.Gly352Arg
NM_000038.6:c.1903G>C MANE Select	NP_000029.2:p.Gly635Arg
NM_001127510.3:c.1903G>C	NP_001120982.1:p.Gly635Arg
NM_001127511.3:c.1849G>C	NP_001120983.2:p.Gly617Arg
NM_001354895.2:c.1903G>C	NP_001341824.1:p.Gly635Arg
NM_001354896.2:c.1957G>C	NP_001341825.1:p.Gly653Arg
NM_001354897.2:c.1933G>C	NP_001341826.1:p.Gly645Arg
NM_001354898.2:c.1828G>C	NP_001341827.1:p.Gly610Arg
NM_001354899.2:c.1819G>C	NP_001341828.1:p.Gly607Arg
NM_001354900.2:c.1780G>C	NP_001341829.1:p.Gly594Arg
NM_001354901.2:c.1726G>C	NP_001341830.1:p.Gly576Arg
NM_001354902.2:c.1630G>C	NP_001341831.1:p.Gly544Arg
NM_001354903.2:c.1600G>C	NP_001341832.1:p.Gly534Arg
NM_001354904.2:c.1525G>C	NP_001341833.1:p.Gly509Arg
NM_001354905.2:c.1423G>C	NP_001341834.1:p.Gly475Arg
NM_001354906.2:c.1054G>C	NP_001341835.1:p.Gly352Arg