Canonical Allele Identifier: CA1573485872

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838673T= , CM000667.2:g.112838673T=	GRCh38
NC_000005.9:g.112174370T= , CM000667.1:g.112174370T=	GRCh37
NC_000005.8:g.112202269T=	NCBI36
NG_008481.4:g.151153T= , LRG_130:g.151153T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2744T=	ENSP00000484935.2:n.2744T=
ENST00000504915.3:c.3133T=	ENSP00000473355.2:p.Tyr1045=
ENST00000505350.2:c.*3085T=	ENSP00000481752.1:n.*3085T=
ENST00000507379.6:c.3025T=	ENSP00000423224.2:p.Tyr1009=
ENST00000509732.6:c.3079T=	ENSP00000426541.2:p.Tyr1027=
ENST00000512211.7:c.3079T=	ENSP00000423828.3:p.Tyr1027=
ENST00000257430.9:c.3079T= MANE Select	ENSP00000257430.4:p.Tyr1027=
ENST00000257430.8:c.3079T=	ENSP00000257430.4:p.Tyr1027=
ENST00000502371.2:c.1432T=
ENST00000507379.5:c.3025T=	ENSP00000423224.1:p.Tyr1009=
ENST00000508376.6:c.3079T=	ENSP00000427089.2:p.Tyr1027=
ENST00000508624.5:c.*2401T=	ENSP00000424265.1:n.*2401T=
ENST00000512211.6:c.3079T=	ENSP00000423828.2:p.Tyr1027=
ENST00000520401.1:c.230+9701T=
NM_000038.5:c.3079T=	NP_000029.2:p.Tyr1027=
NM_001127510.2:c.3079T=	NP_001120982.1:p.Tyr1027=
NM_001127511.2:c.3025T=	NP_001120983.2:p.Tyr1009=
NM_001354895.1:c.3079T=	NP_001341824.1:p.Tyr1027=
NM_001354896.1:c.3133T=	NP_001341825.1:p.Tyr1045=
NM_001354897.1:c.3109T=	NP_001341826.1:p.Tyr1037=
NM_001354898.1:c.3004T=	NP_001341827.1:p.Tyr1002=
NM_001354899.1:c.2995T=	NP_001341828.1:p.Tyr999=
NM_001354900.1:c.2956T=	NP_001341829.1:p.Tyr986=
NM_001354901.1:c.2902T=	NP_001341830.1:p.Tyr968=
NM_001354902.1:c.2806T=	NP_001341831.1:p.Tyr936=
NM_001354903.1:c.2776T=	NP_001341832.1:p.Tyr926=
NM_001354904.1:c.2701T=	NP_001341833.1:p.Tyr901=
NM_001354905.1:c.2599T=	NP_001341834.1:p.Tyr867=
NM_001354906.1:c.2230T=	NP_001341835.1:p.Tyr744=
NM_000038.6:c.3079T= MANE Select	NP_000029.2:p.Tyr1027=
NM_001127510.3:c.3079T=	NP_001120982.1:p.Tyr1027=
NM_001127511.3:c.3025T=	NP_001120983.2:p.Tyr1009=
NM_001354895.2:c.3079T=	NP_001341824.1:p.Tyr1027=
NM_001354896.2:c.3133T=	NP_001341825.1:p.Tyr1045=
NM_001354897.2:c.3109T=	NP_001341826.1:p.Tyr1037=
NM_001354898.2:c.3004T=	NP_001341827.1:p.Tyr1002=
NM_001354899.2:c.2995T=	NP_001341828.1:p.Tyr999=
NM_001354900.2:c.2956T=	NP_001341829.1:p.Tyr986=
NM_001354901.2:c.2902T=	NP_001341830.1:p.Tyr968=
NM_001354902.2:c.2806T=	NP_001341831.1:p.Tyr936=
NM_001354903.2:c.2776T=	NP_001341832.1:p.Tyr926=
NM_001354904.2:c.2701T=	NP_001341833.1:p.Tyr901=
NM_001354905.2:c.2599T=	NP_001341834.1:p.Tyr867=
NM_001354906.2:c.2230T=	NP_001341835.1:p.Tyr744=