Canonical Allele Identifier: CA3124061241

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112841156C= , CM000667.2:g.112841156C=	GRCh38
NC_000005.9:g.112176853C= , CM000667.1:g.112176853C=	GRCh37
NC_000005.8:g.112204752C=	NCBI36
NG_008481.4:g.153636C= , LRG_130:g.153636C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.5562C= MANE Select	NP_000029.2:p.Tyr1854=
ENST00000257430.9:c.5562C= MANE Select	ENSP00000257430.4:p.Tyr1854=
NM_000038.5:c.5562C=	NP_000029.2:p.Tyr1854=
NM_001127510.2:c.5562C=	NP_001120982.1:p.Tyr1854=
NM_001127510.3:c.5562C=	NP_001120982.1:p.Tyr1854=
NM_001127511.2:c.5508C=	NP_001120983.2:p.Tyr1836=
NM_001127511.3:c.5508C=	NP_001120983.2:p.Tyr1836=
NM_001354895.1:c.5562C=	NP_001341824.1:p.Tyr1854=
NM_001354895.2:c.5562C=	NP_001341824.1:p.Tyr1854=
NM_001354896.1:c.5616C=	NP_001341825.1:p.Tyr1872=
NM_001354896.2:c.5616C=	NP_001341825.1:p.Tyr1872=
NM_001354897.1:c.5592C=	NP_001341826.1:p.Tyr1864=
NM_001354897.2:c.5592C=	NP_001341826.1:p.Tyr1864=
NM_001354898.1:c.5487C=	NP_001341827.1:p.Tyr1829=
NM_001354898.2:c.5487C=	NP_001341827.1:p.Tyr1829=
NM_001354899.1:c.5478C=	NP_001341828.1:p.Tyr1826=
NM_001354899.2:c.5478C=	NP_001341828.1:p.Tyr1826=
NM_001354900.1:c.5439C=	NP_001341829.1:p.Tyr1813=
NM_001354900.2:c.5439C=	NP_001341829.1:p.Tyr1813=
NM_001354901.1:c.5385C=	NP_001341830.1:p.Tyr1795=
NM_001354901.2:c.5385C=	NP_001341830.1:p.Tyr1795=
NM_001354902.1:c.5289C=	NP_001341831.1:p.Tyr1763=
NM_001354902.2:c.5289C=	NP_001341831.1:p.Tyr1763=
NM_001354903.1:c.5259C=	NP_001341832.1:p.Tyr1753=
NM_001354903.2:c.5259C=	NP_001341832.1:p.Tyr1753=
NM_001354904.1:c.5184C=	NP_001341833.1:p.Tyr1728=
NM_001354904.2:c.5184C=	NP_001341833.1:p.Tyr1728=
NM_001354905.1:c.5082C=	NP_001341834.1:p.Tyr1694=
NM_001354905.2:c.5082C=	NP_001341834.1:p.Tyr1694=
NM_001354906.1:c.4713C=	NP_001341835.1:p.Tyr1571=
NM_001354906.2:c.4713C=	NP_001341835.1:p.Tyr1571=
ENST00000257430.8:c.5562C=	ENSP00000257430.4:p.Tyr1854=
ENST00000504915.3:c.5616C=	ENSP00000473355.2:p.Tyr1872=
ENST00000505350.2:c.*5568C=	ENSP00000481752.1:n.*5568C=
ENST00000507379.6:c.5508C=	ENSP00000423224.2:p.Tyr1836=
ENST00000508376.6:c.5562C=	ENSP00000427089.2:p.Tyr1854=
ENST00000508624.5:c.*4884C=	ENSP00000424265.1:n.*4884C=
ENST00000509732.6:c.5562C=	ENSP00000426541.2:p.Tyr1854=
ENST00000512211.7:c.5562C=	ENSP00000423828.3:p.Tyr1854=
ENST00000520401.1:c.230+12184C=