Canonical Allele Identifier: CA445963684

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839359C>T , CM000667.2:g.112839359C>T	GRCh38
NC_000005.9:g.112175056C>T , CM000667.1:g.112175056C>T	GRCh37
NC_000005.8:g.112202955C>T	NCBI36
NG_008481.4:g.151839C>T , LRG_130:g.151839C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.3765C>T MANE Select	NP_000029.2:p.Asn1255=
ENST00000257430.9:c.3765C>T MANE Select	ENSP00000257430.4:p.Asn1255=
NM_000038.5:c.3765C>T	NP_000029.2:p.Asn1255=
NM_001127510.2:c.3765C>T	NP_001120982.1:p.Asn1255=
NM_001127510.3:c.3765C>T	NP_001120982.1:p.Asn1255=
NM_001127511.2:c.3711C>T	NP_001120983.2:p.Asn1237=
NM_001127511.3:c.3711C>T	NP_001120983.2:p.Asn1237=
NM_001354895.1:c.3765C>T	NP_001341824.1:p.Asn1255=
NM_001354895.2:c.3765C>T	NP_001341824.1:p.Asn1255=
NM_001354896.1:c.3819C>T	NP_001341825.1:p.Asn1273=
NM_001354896.2:c.3819C>T	NP_001341825.1:p.Asn1273=
NM_001354897.1:c.3795C>T	NP_001341826.1:p.Asn1265=
NM_001354897.2:c.3795C>T	NP_001341826.1:p.Asn1265=
NM_001354898.1:c.3690C>T	NP_001341827.1:p.Asn1230=
NM_001354898.2:c.3690C>T	NP_001341827.1:p.Asn1230=
NM_001354899.1:c.3681C>T	NP_001341828.1:p.Asn1227=
NM_001354899.2:c.3681C>T	NP_001341828.1:p.Asn1227=
NM_001354900.1:c.3642C>T	NP_001341829.1:p.Asn1214=
NM_001354900.2:c.3642C>T	NP_001341829.1:p.Asn1214=
NM_001354901.1:c.3588C>T	NP_001341830.1:p.Asn1196=
NM_001354901.2:c.3588C>T	NP_001341830.1:p.Asn1196=
NM_001354902.1:c.3492C>T	NP_001341831.1:p.Asn1164=
NM_001354902.2:c.3492C>T	NP_001341831.1:p.Asn1164=
NM_001354903.1:c.3462C>T	NP_001341832.1:p.Asn1154=
NM_001354903.2:c.3462C>T	NP_001341832.1:p.Asn1154=
NM_001354904.1:c.3387C>T	NP_001341833.1:p.Asn1129=
NM_001354904.2:c.3387C>T	NP_001341833.1:p.Asn1129=
NM_001354905.1:c.3285C>T	NP_001341834.1:p.Asn1095=
NM_001354905.2:c.3285C>T	NP_001341834.1:p.Asn1095=
NM_001354906.1:c.2916C>T	NP_001341835.1:p.Asn972=
NM_001354906.2:c.2916C>T	NP_001341835.1:p.Asn972=
ENST00000257430.8:c.3765C>T	ENSP00000257430.4:p.Asn1255=
ENST00000502371.2:c.2118C>T
ENST00000502371.3:c.3430C>T	ENSP00000484935.2:n.3430C>T
ENST00000504915.3:c.3819C>T	ENSP00000473355.2:p.Asn1273=
ENST00000505350.2:c.*3771C>T	ENSP00000481752.1:n.*3771C>T
ENST00000507379.6:c.3711C>T	ENSP00000423224.2:p.Asn1237=
ENST00000508376.6:c.3765C>T	ENSP00000427089.2:p.Asn1255=
ENST00000508624.5:c.*3087C>T	ENSP00000424265.1:n.*3087C>T
ENST00000509732.6:c.3765C>T	ENSP00000426541.2:p.Asn1255=
ENST00000512211.6:c.3765C>T	ENSP00000423828.2:p.Asn1255=
ENST00000512211.7:c.3765C>T	ENSP00000423828.3:p.Asn1255=
ENST00000520401.1:c.230+10387C>T