Canonical Allele Identifier: CA1573497050

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112821896T= , CM000667.2:g.112821896T=	GRCh38
NC_000005.9:g.112157593T= , CM000667.1:g.112157593T=	GRCh37
NC_000005.8:g.112185492T=	NCBI36
NG_008481.4:g.134376T= , LRG_130:g.134376T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1313T=	ENSP00000484935.2:p.Met438=
ENST00000504915.3:c.1313T=	ENSP00000473355.2:p.Met438=
ENST00000505084.2:n.1369T=
ENST00000505350.2:c.*1319T=	ENSP00000481752.1:n.*1319T=
ENST00000507379.6:c.1259T=	ENSP00000423224.2:p.Met420=
ENST00000509732.6:c.1313T=	ENSP00000426541.2:p.Met438=
ENST00000512211.7:c.1313T=	ENSP00000423828.3:p.Met438=
ENST00000257430.9:c.1313T= MANE Select	ENSP00000257430.4:p.Met438=
ENST00000257430.8:c.1313T=	ENSP00000257430.4:p.Met438=
ENST00000502371.2:c.1T=
ENST00000507379.5:c.1259T=	ENSP00000423224.1:p.Met420=
ENST00000508376.6:c.1313T=	ENSP00000427089.2:p.Met438=
ENST00000508624.5:c.*635T=	ENSP00000424265.1:n.*635T=
ENST00000512211.6:c.1313T=	ENSP00000423828.2:p.Met438=
NM_000038.5:c.1313T=	NP_000029.2:p.Met438=
NM_001127510.2:c.1313T=	NP_001120982.1:p.Met438=
NM_001127511.2:c.1259T=	NP_001120983.2:p.Met420=
NM_001354895.1:c.1313T=	NP_001341824.1:p.Met438=
NM_001354896.1:c.1313T=	NP_001341825.1:p.Met438=
NM_001354897.1:c.1343T=	NP_001341826.1:p.Met448=
NM_001354898.1:c.1238T=	NP_001341827.1:p.Met413=
NM_001354899.1:c.1229T=	NP_001341828.1:p.Met410=
NM_001354900.1:c.1136T=	NP_001341829.1:p.Met379=
NM_001354901.1:c.1136T=	NP_001341830.1:p.Met379=
NM_001354902.1:c.1040T=	NP_001341831.1:p.Met347=
NM_001354903.1:c.1010T=	NP_001341832.1:p.Met337=
NM_001354904.1:c.935T=	NP_001341833.1:p.Met312=
NM_001354905.1:c.833T=	NP_001341834.1:p.Met278=
NM_001354906.1:c.464T=	NP_001341835.1:p.Met155=
NM_000038.6:c.1313T= MANE Select	NP_000029.2:p.Met438=
NM_001127510.3:c.1313T=	NP_001120982.1:p.Met438=
NM_001127511.3:c.1259T=	NP_001120983.2:p.Met420=
NM_001354895.2:c.1313T=	NP_001341824.1:p.Met438=
NM_001354896.2:c.1313T=	NP_001341825.1:p.Met438=
NM_001354897.2:c.1343T=	NP_001341826.1:p.Met448=
NM_001354898.2:c.1238T=	NP_001341827.1:p.Met413=
NM_001354899.2:c.1229T=	NP_001341828.1:p.Met410=
NM_001354900.2:c.1136T=	NP_001341829.1:p.Met379=
NM_001354901.2:c.1136T=	NP_001341830.1:p.Met379=
NM_001354902.2:c.1040T=	NP_001341831.1:p.Met347=
NM_001354903.2:c.1010T=	NP_001341832.1:p.Met337=
NM_001354904.2:c.935T=	NP_001341833.1:p.Met312=
NM_001354905.2:c.833T=	NP_001341834.1:p.Met278=
NM_001354906.2:c.464T=	NP_001341835.1:p.Met155=