Canonical Allele Identifier: CA16031623

Gene: APC

Linked Data

• dbSNP Id: rs1343192266
• MyVariant Identifiers: chr5:g.112175985A>T (hg19) ; chr5:g.112840288A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840288A>T , CM000667.2:g.112840288A>T	GRCh38
NC_000005.9:g.112175985A>T , CM000667.1:g.112175985A>T	GRCh37
NC_000005.8:g.112203884A>T	NCBI36
NG_008481.4:g.152768A>T , LRG_130:g.152768A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4748A>T	ENSP00000473355.2:p.Asp1583Val
ENST00000505350.2:c.*4700A>T	ENSP00000481752.1:n.*4700A>T
ENST00000507379.6:c.4640A>T	ENSP00000423224.2:p.Asp1547Val
ENST00000509732.6:c.4694A>T	ENSP00000426541.2:p.Asp1565Val
ENST00000512211.7:c.4694A>T	ENSP00000423828.3:p.Asp1565Val
ENST00000257430.9:c.4694A>T MANE Select	ENSP00000257430.4:p.Asp1565Val
ENST00000257430.8:c.4694A>T	ENSP00000257430.4:p.Asp1565Val
ENST00000508376.6:c.4694A>T	ENSP00000427089.2:p.Asp1565Val
ENST00000508624.5:c.*4016A>T	ENSP00000424265.1:n.*4016A>T
ENST00000520401.1:c.230+11316A>T
NM_000038.5:c.4694A>T	NP_000029.2:p.Asp1565Val
NM_001127510.2:c.4694A>T	NP_001120982.1:p.Asp1565Val
NM_001127511.2:c.4640A>T	NP_001120983.2:p.Asp1547Val
NM_001354895.1:c.4694A>T	NP_001341824.1:p.Asp1565Val
NM_001354896.1:c.4748A>T	NP_001341825.1:p.Asp1583Val
NM_001354897.1:c.4724A>T	NP_001341826.1:p.Asp1575Val
NM_001354898.1:c.4619A>T	NP_001341827.1:p.Asp1540Val
NM_001354899.1:c.4610A>T	NP_001341828.1:p.Asp1537Val
NM_001354900.1:c.4571A>T	NP_001341829.1:p.Asp1524Val
NM_001354901.1:c.4517A>T	NP_001341830.1:p.Asp1506Val
NM_001354902.1:c.4421A>T	NP_001341831.1:p.Asp1474Val
NM_001354903.1:c.4391A>T	NP_001341832.1:p.Asp1464Val
NM_001354904.1:c.4316A>T	NP_001341833.1:p.Asp1439Val
NM_001354905.1:c.4214A>T	NP_001341834.1:p.Asp1405Val
NM_001354906.1:c.3845A>T	NP_001341835.1:p.Asp1282Val
NM_000038.6:c.4694A>T MANE Select	NP_000029.2:p.Asp1565Val
NM_001127510.3:c.4694A>T	NP_001120982.1:p.Asp1565Val
NM_001127511.3:c.4640A>T	NP_001120983.2:p.Asp1547Val
NM_001354895.2:c.4694A>T	NP_001341824.1:p.Asp1565Val
NM_001354896.2:c.4748A>T	NP_001341825.1:p.Asp1583Val
NM_001354897.2:c.4724A>T	NP_001341826.1:p.Asp1575Val
NM_001354898.2:c.4619A>T	NP_001341827.1:p.Asp1540Val
NM_001354899.2:c.4610A>T	NP_001341828.1:p.Asp1537Val
NM_001354900.2:c.4571A>T	NP_001341829.1:p.Asp1524Val
NM_001354901.2:c.4517A>T	NP_001341830.1:p.Asp1506Val
NM_001354902.2:c.4421A>T	NP_001341831.1:p.Asp1474Val
NM_001354903.2:c.4391A>T	NP_001341832.1:p.Asp1464Val
NM_001354904.2:c.4316A>T	NP_001341833.1:p.Asp1439Val
NM_001354905.2:c.4214A>T	NP_001341834.1:p.Asp1405Val
NM_001354906.2:c.3845A>T	NP_001341835.1:p.Asp1282Val