Canonical Allele Identifier: CA16031657

Gene: APC

Linked Data

• dbSNP Id: rs1267672358
• MyVariant Identifiers: chr5:g.112175999G>T (hg19) ; chr5:g.112840302G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840302G>T , CM000667.2:g.112840302G>T	GRCh38
NC_000005.9:g.112175999G>T , CM000667.1:g.112175999G>T	GRCh37
NC_000005.8:g.112203898G>T	NCBI36
NG_008481.4:g.152782G>T , LRG_130:g.152782G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4762G>T	ENSP00000473355.2:p.Asp1588Tyr
ENST00000505350.2:c.*4714G>T	ENSP00000481752.1:n.*4714G>T
ENST00000507379.6:c.4654G>T	ENSP00000423224.2:p.Asp1552Tyr
ENST00000509732.6:c.4708G>T	ENSP00000426541.2:p.Asp1570Tyr
ENST00000512211.7:c.4708G>T	ENSP00000423828.3:p.Asp1570Tyr
ENST00000257430.9:c.4708G>T MANE Select	ENSP00000257430.4:p.Asp1570Tyr
ENST00000257430.8:c.4708G>T	ENSP00000257430.4:p.Asp1570Tyr
ENST00000508376.6:c.4708G>T	ENSP00000427089.2:p.Asp1570Tyr
ENST00000508624.5:c.*4030G>T	ENSP00000424265.1:n.*4030G>T
ENST00000520401.1:c.230+11330G>T
NM_000038.5:c.4708G>T	NP_000029.2:p.Asp1570Tyr
NM_001127510.2:c.4708G>T	NP_001120982.1:p.Asp1570Tyr
NM_001127511.2:c.4654G>T	NP_001120983.2:p.Asp1552Tyr
NM_001354895.1:c.4708G>T	NP_001341824.1:p.Asp1570Tyr
NM_001354896.1:c.4762G>T	NP_001341825.1:p.Asp1588Tyr
NM_001354897.1:c.4738G>T	NP_001341826.1:p.Asp1580Tyr
NM_001354898.1:c.4633G>T	NP_001341827.1:p.Asp1545Tyr
NM_001354899.1:c.4624G>T	NP_001341828.1:p.Asp1542Tyr
NM_001354900.1:c.4585G>T	NP_001341829.1:p.Asp1529Tyr
NM_001354901.1:c.4531G>T	NP_001341830.1:p.Asp1511Tyr
NM_001354902.1:c.4435G>T	NP_001341831.1:p.Asp1479Tyr
NM_001354903.1:c.4405G>T	NP_001341832.1:p.Asp1469Tyr
NM_001354904.1:c.4330G>T	NP_001341833.1:p.Asp1444Tyr
NM_001354905.1:c.4228G>T	NP_001341834.1:p.Asp1410Tyr
NM_001354906.1:c.3859G>T	NP_001341835.1:p.Asp1287Tyr
NM_000038.6:c.4708G>T MANE Select	NP_000029.2:p.Asp1570Tyr
NM_001127510.3:c.4708G>T	NP_001120982.1:p.Asp1570Tyr
NM_001127511.3:c.4654G>T	NP_001120983.2:p.Asp1552Tyr
NM_001354895.2:c.4708G>T	NP_001341824.1:p.Asp1570Tyr
NM_001354896.2:c.4762G>T	NP_001341825.1:p.Asp1588Tyr
NM_001354897.2:c.4738G>T	NP_001341826.1:p.Asp1580Tyr
NM_001354898.2:c.4633G>T	NP_001341827.1:p.Asp1545Tyr
NM_001354899.2:c.4624G>T	NP_001341828.1:p.Asp1542Tyr
NM_001354900.2:c.4585G>T	NP_001341829.1:p.Asp1529Tyr
NM_001354901.2:c.4531G>T	NP_001341830.1:p.Asp1511Tyr
NM_001354902.2:c.4435G>T	NP_001341831.1:p.Asp1479Tyr
NM_001354903.2:c.4405G>T	NP_001341832.1:p.Asp1469Tyr
NM_001354904.2:c.4330G>T	NP_001341833.1:p.Asp1444Tyr
NM_001354905.2:c.4228G>T	NP_001341834.1:p.Asp1410Tyr
NM_001354906.2:c.3859G>T	NP_001341835.1:p.Asp1287Tyr