Canonical Allele Identifier: CA10578317

Gene: APC

Linked Data

• ClinVar Variation Id: 230854
• ClinVar RCV Id: RCV003765410 ; RCV000220669
• dbSNP Id: rs876658811
• MyVariant Identifiers: chr5:g.112162927G>T (hg19) ; chr5:g.112827230G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112827230G>T , CM000667.2:g.112827230G>T	GRCh38
NC_000005.9:g.112162927G>T , CM000667.1:g.112162927G>T	GRCh37
NC_000005.8:g.112190826G>T	NCBI36
NG_008481.4:g.139710G>T , LRG_130:g.139710G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1408+5239G>T	ENSP00000484935.2:n.1408+5239G>T
ENST00000504915.3:c.1585G>T	ENSP00000473355.2:p.Gly529Ter
ENST00000505084.2:n.1587G>T
ENST00000505350.2:c.*1537G>T	ENSP00000481752.1:n.*1537G>T
ENST00000507379.6:c.1477G>T	ENSP00000423224.2:p.Gly493Ter
ENST00000509732.6:c.1531G>T	ENSP00000426541.2:p.Gly511Ter
ENST00000512211.7:c.1531G>T	ENSP00000423828.3:p.Gly511Ter
ENST00000257430.9:c.1531G>T MANE Select	ENSP00000257430.4:p.Gly511Ter
ENST00000257430.8:c.1531G>T	ENSP00000257430.4:p.Gly511Ter
ENST00000502371.2:c.96+5239G>T
ENST00000504915.2:c.220G>T	ENSP00000473355.1:p.Gly74Ter
ENST00000505084.1:n.18G>T
ENST00000507379.5:c.1477G>T	ENSP00000423224.1:p.Gly493Ter
ENST00000508376.6:c.1531G>T	ENSP00000427089.2:p.Gly511Ter
ENST00000508624.5:c.*853G>T	ENSP00000424265.1:n.*853G>T
ENST00000512211.6:c.1531G>T	ENSP00000423828.2:p.Gly511Ter
ENST00000520401.1:c.18G>T
NM_000038.5:c.1531G>T	NP_000029.2:p.Gly511Ter
NM_001127510.2:c.1531G>T	NP_001120982.1:p.Gly511Ter
NM_001127511.2:c.1477G>T	NP_001120983.2:p.Gly493Ter
NM_001354895.1:c.1531G>T	NP_001341824.1:p.Gly511Ter
NM_001354896.1:c.1585G>T	NP_001341825.1:p.Gly529Ter
NM_001354897.1:c.1561G>T	NP_001341826.1:p.Gly521Ter
NM_001354898.1:c.1456G>T	NP_001341827.1:p.Gly486Ter
NM_001354899.1:c.1447G>T	NP_001341828.1:p.Gly483Ter
NM_001354900.1:c.1408G>T	NP_001341829.1:p.Gly470Ter
NM_001354901.1:c.1354G>T	NP_001341830.1:p.Gly452Ter
NM_001354902.1:c.1258G>T	NP_001341831.1:p.Gly420Ter
NM_001354903.1:c.1228G>T	NP_001341832.1:p.Gly410Ter
NM_001354904.1:c.1153G>T	NP_001341833.1:p.Gly385Ter
NM_001354905.1:c.1051G>T	NP_001341834.1:p.Gly351Ter
NM_001354906.1:c.682G>T	NP_001341835.1:p.Gly228Ter
NM_000038.6:c.1531G>T MANE Select	NP_000029.2:p.Gly511Ter
NM_001127510.3:c.1531G>T	NP_001120982.1:p.Gly511Ter
NM_001127511.3:c.1477G>T	NP_001120983.2:p.Gly493Ter
NM_001354895.2:c.1531G>T	NP_001341824.1:p.Gly511Ter
NM_001354896.2:c.1585G>T	NP_001341825.1:p.Gly529Ter
NM_001354897.2:c.1561G>T	NP_001341826.1:p.Gly521Ter
NM_001354898.2:c.1456G>T	NP_001341827.1:p.Gly486Ter
NM_001354899.2:c.1447G>T	NP_001341828.1:p.Gly483Ter
NM_001354900.2:c.1408G>T	NP_001341829.1:p.Gly470Ter
NM_001354901.2:c.1354G>T	NP_001341830.1:p.Gly452Ter
NM_001354902.2:c.1258G>T	NP_001341831.1:p.Gly420Ter
NM_001354903.2:c.1228G>T	NP_001341832.1:p.Gly410Ter
NM_001354904.2:c.1153G>T	NP_001341833.1:p.Gly385Ter
NM_001354905.2:c.1051G>T	NP_001341834.1:p.Gly351Ter
NM_001354906.2:c.682G>T	NP_001341835.1:p.Gly228Ter