Canonical Allele Identifier: CA1573470937

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840289T= , CM000667.2:g.112840289T=	GRCh38
NC_000005.9:g.112175986T= , CM000667.1:g.112175986T=	GRCh37
NC_000005.8:g.112203885T=	NCBI36
NG_008481.4:g.152769T= , LRG_130:g.152769T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4749T=	ENSP00000473355.2:p.Asp1583=
ENST00000505350.2:c.*4701T=	ENSP00000481752.1:n.*4701T=
ENST00000507379.6:c.4641T=	ENSP00000423224.2:p.Asp1547=
ENST00000509732.6:c.4695T=	ENSP00000426541.2:p.Asp1565=
ENST00000512211.7:c.4695T=	ENSP00000423828.3:p.Asp1565=
ENST00000257430.9:c.4695T= MANE Select	ENSP00000257430.4:p.Asp1565=
ENST00000257430.8:c.4695T=	ENSP00000257430.4:p.Asp1565=
ENST00000508376.6:c.4695T=	ENSP00000427089.2:p.Asp1565=
ENST00000508624.5:c.*4017T=	ENSP00000424265.1:n.*4017T=
ENST00000520401.1:c.230+11317T=
NM_000038.5:c.4695T=	NP_000029.2:p.Asp1565=
NM_001127510.2:c.4695T=	NP_001120982.1:p.Asp1565=
NM_001127511.2:c.4641T=	NP_001120983.2:p.Asp1547=
NM_001354895.1:c.4695T=	NP_001341824.1:p.Asp1565=
NM_001354896.1:c.4749T=	NP_001341825.1:p.Asp1583=
NM_001354897.1:c.4725T=	NP_001341826.1:p.Asp1575=
NM_001354898.1:c.4620T=	NP_001341827.1:p.Asp1540=
NM_001354899.1:c.4611T=	NP_001341828.1:p.Asp1537=
NM_001354900.1:c.4572T=	NP_001341829.1:p.Asp1524=
NM_001354901.1:c.4518T=	NP_001341830.1:p.Asp1506=
NM_001354902.1:c.4422T=	NP_001341831.1:p.Asp1474=
NM_001354903.1:c.4392T=	NP_001341832.1:p.Asp1464=
NM_001354904.1:c.4317T=	NP_001341833.1:p.Asp1439=
NM_001354905.1:c.4215T=	NP_001341834.1:p.Asp1405=
NM_001354906.1:c.3846T=	NP_001341835.1:p.Asp1282=
NM_000038.6:c.4695T= MANE Select	NP_000029.2:p.Asp1565=
NM_001127510.3:c.4695T=	NP_001120982.1:p.Asp1565=
NM_001127511.3:c.4641T=	NP_001120983.2:p.Asp1547=
NM_001354895.2:c.4695T=	NP_001341824.1:p.Asp1565=
NM_001354896.2:c.4749T=	NP_001341825.1:p.Asp1583=
NM_001354897.2:c.4725T=	NP_001341826.1:p.Asp1575=
NM_001354898.2:c.4620T=	NP_001341827.1:p.Asp1540=
NM_001354899.2:c.4611T=	NP_001341828.1:p.Asp1537=
NM_001354900.2:c.4572T=	NP_001341829.1:p.Asp1524=
NM_001354901.2:c.4518T=	NP_001341830.1:p.Asp1506=
NM_001354902.2:c.4422T=	NP_001341831.1:p.Asp1474=
NM_001354903.2:c.4392T=	NP_001341832.1:p.Asp1464=
NM_001354904.2:c.4317T=	NP_001341833.1:p.Asp1439=
NM_001354905.2:c.4215T=	NP_001341834.1:p.Asp1405=
NM_001354906.2:c.3846T=	NP_001341835.1:p.Asp1282=