Canonical Allele Identifier: CA16037696

Gene: APC

Linked Data

• dbSNP Id: rs730881263
• MyVariant Identifiers: chr5:g.112178819A>T (hg19) ; chr5:g.112843122A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843122A>T , CM000667.2:g.112843122A>T	GRCh38
NC_000005.9:g.112178819A>T , CM000667.1:g.112178819A>T	GRCh37
NC_000005.8:g.112206718A>T	NCBI36
NG_008481.4:g.155602A>T , LRG_130:g.155602A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.7582A>T	ENSP00000473355.2:p.Asn2528Tyr
ENST00000505350.2:c.*7534A>T	ENSP00000481752.1:n.*7534A>T
ENST00000507379.6:c.7474A>T	ENSP00000423224.2:p.Asn2492Tyr
ENST00000509732.6:c.7528A>T	ENSP00000426541.2:p.Asn2510Tyr
ENST00000512211.7:c.7528A>T	ENSP00000423828.3:p.Asn2510Tyr
ENST00000257430.9:c.7528A>T MANE Select	ENSP00000257430.4:p.Asn2510Tyr
ENST00000257430.8:c.7528A>T	ENSP00000257430.4:p.Asn2510Tyr
ENST00000508376.6:c.7528A>T	ENSP00000427089.2:p.Asn2510Tyr
ENST00000520401.1:c.231-13527A>T
NM_000038.5:c.7528A>T	NP_000029.2:p.Asn2510Tyr
NM_001127510.2:c.7528A>T	NP_001120982.1:p.Asn2510Tyr
NM_001127511.2:c.7474A>T	NP_001120983.2:p.Asn2492Tyr
NM_001354895.1:c.7528A>T	NP_001341824.1:p.Asn2510Tyr
NM_001354896.1:c.7582A>T	NP_001341825.1:p.Asn2528Tyr
NM_001354897.1:c.7558A>T	NP_001341826.1:p.Asn2520Tyr
NM_001354898.1:c.7453A>T	NP_001341827.1:p.Asn2485Tyr
NM_001354899.1:c.7444A>T	NP_001341828.1:p.Asn2482Tyr
NM_001354900.1:c.7405A>T	NP_001341829.1:p.Asn2469Tyr
NM_001354901.1:c.7351A>T	NP_001341830.1:p.Asn2451Tyr
NM_001354902.1:c.7255A>T	NP_001341831.1:p.Asn2419Tyr
NM_001354903.1:c.7225A>T	NP_001341832.1:p.Asn2409Tyr
NM_001354904.1:c.7150A>T	NP_001341833.1:p.Asn2384Tyr
NM_001354905.1:c.7048A>T	NP_001341834.1:p.Asn2350Tyr
NM_001354906.1:c.6679A>T	NP_001341835.1:p.Asn2227Tyr
NM_000038.6:c.7528A>T MANE Select	NP_000029.2:p.Asn2510Tyr
NM_001127510.3:c.7528A>T	NP_001120982.1:p.Asn2510Tyr
NM_001127511.3:c.7474A>T	NP_001120983.2:p.Asn2492Tyr
NM_001354895.2:c.7528A>T	NP_001341824.1:p.Asn2510Tyr
NM_001354896.2:c.7582A>T	NP_001341825.1:p.Asn2528Tyr
NM_001354897.2:c.7558A>T	NP_001341826.1:p.Asn2520Tyr
NM_001354898.2:c.7453A>T	NP_001341827.1:p.Asn2485Tyr
NM_001354899.2:c.7444A>T	NP_001341828.1:p.Asn2482Tyr
NM_001354900.2:c.7405A>T	NP_001341829.1:p.Asn2469Tyr
NM_001354901.2:c.7351A>T	NP_001341830.1:p.Asn2451Tyr
NM_001354902.2:c.7255A>T	NP_001341831.1:p.Asn2419Tyr
NM_001354903.2:c.7225A>T	NP_001341832.1:p.Asn2409Tyr
NM_001354904.2:c.7150A>T	NP_001341833.1:p.Asn2384Tyr
NM_001354905.2:c.7048A>T	NP_001341834.1:p.Asn2350Tyr
NM_001354906.2:c.6679A>T	NP_001341835.1:p.Asn2227Tyr