Canonical Allele Identifier: CA1573485553

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838626C= , CM000667.2:g.112838626C=	GRCh38
NC_000005.9:g.112174323C= , CM000667.1:g.112174323C=	GRCh37
NC_000005.8:g.112202222C=	NCBI36
NG_008481.4:g.151106C= , LRG_130:g.151106C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2697C=	ENSP00000484935.2:n.2697C=
ENST00000504915.3:c.3086C=	ENSP00000473355.2:p.Ala1029=
ENST00000505350.2:c.*3038C=	ENSP00000481752.1:n.*3038C=
ENST00000507379.6:c.2978C=	ENSP00000423224.2:p.Ala993=
ENST00000509732.6:c.3032C=	ENSP00000426541.2:p.Ala1011=
ENST00000512211.7:c.3032C=	ENSP00000423828.3:p.Ala1011=
ENST00000257430.9:c.3032C= MANE Select	ENSP00000257430.4:p.Ala1011=
ENST00000257430.8:c.3032C=	ENSP00000257430.4:p.Ala1011=
ENST00000502371.2:c.1385C=
ENST00000507379.5:c.2978C=	ENSP00000423224.1:p.Ala993=
ENST00000508376.6:c.3032C=	ENSP00000427089.2:p.Ala1011=
ENST00000508624.5:c.*2354C=	ENSP00000424265.1:n.*2354C=
ENST00000512211.6:c.3032C=	ENSP00000423828.2:p.Ala1011=
ENST00000520401.1:c.230+9654C=
NM_000038.5:c.3032C=	NP_000029.2:p.Ala1011=
NM_001127510.2:c.3032C=	NP_001120982.1:p.Ala1011=
NM_001127511.2:c.2978C=	NP_001120983.2:p.Ala993=
NM_001354895.1:c.3032C=	NP_001341824.1:p.Ala1011=
NM_001354896.1:c.3086C=	NP_001341825.1:p.Ala1029=
NM_001354897.1:c.3062C=	NP_001341826.1:p.Ala1021=
NM_001354898.1:c.2957C=	NP_001341827.1:p.Ala986=
NM_001354899.1:c.2948C=	NP_001341828.1:p.Ala983=
NM_001354900.1:c.2909C=	NP_001341829.1:p.Ala970=
NM_001354901.1:c.2855C=	NP_001341830.1:p.Ala952=
NM_001354902.1:c.2759C=	NP_001341831.1:p.Ala920=
NM_001354903.1:c.2729C=	NP_001341832.1:p.Ala910=
NM_001354904.1:c.2654C=	NP_001341833.1:p.Ala885=
NM_001354905.1:c.2552C=	NP_001341834.1:p.Ala851=
NM_001354906.1:c.2183C=	NP_001341835.1:p.Ala728=
NM_000038.6:c.3032C= MANE Select	NP_000029.2:p.Ala1011=
NM_001127510.3:c.3032C=	NP_001120982.1:p.Ala1011=
NM_001127511.3:c.2978C=	NP_001120983.2:p.Ala993=
NM_001354895.2:c.3032C=	NP_001341824.1:p.Ala1011=
NM_001354896.2:c.3086C=	NP_001341825.1:p.Ala1029=
NM_001354897.2:c.3062C=	NP_001341826.1:p.Ala1021=
NM_001354898.2:c.2957C=	NP_001341827.1:p.Ala986=
NM_001354899.2:c.2948C=	NP_001341828.1:p.Ala983=
NM_001354900.2:c.2909C=	NP_001341829.1:p.Ala970=
NM_001354901.2:c.2855C=	NP_001341830.1:p.Ala952=
NM_001354902.2:c.2759C=	NP_001341831.1:p.Ala920=
NM_001354903.2:c.2729C=	NP_001341832.1:p.Ala910=
NM_001354904.2:c.2654C=	NP_001341833.1:p.Ala885=
NM_001354905.2:c.2552C=	NP_001341834.1:p.Ala851=
NM_001354906.2:c.2183C=	NP_001341835.1:p.Ala728=