Canonical Allele Identifier: CA445963174

Gene: APC

Linked Data

• dbSNP Id: rs2149884230
• MyVariant Identifiers: chr5:g.112174387A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838690A>T , CM000667.2:g.112838690A>T	GRCh38
NC_000005.9:g.112174387A>T , CM000667.1:g.112174387A>T	GRCh37
NC_000005.8:g.112202286A>T	NCBI36
NG_008481.4:g.151170A>T , LRG_130:g.151170A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2761A>T	ENSP00000484935.2:n.2761A>T
ENST00000504915.3:c.3150A>T	ENSP00000473355.2:p.Ser1050=
ENST00000505350.2:c.*3102A>T	ENSP00000481752.1:n.*3102A>T
ENST00000507379.6:c.3042A>T	ENSP00000423224.2:p.Ser1014=
ENST00000509732.6:c.3096A>T	ENSP00000426541.2:p.Ser1032=
ENST00000512211.7:c.3096A>T	ENSP00000423828.3:p.Ser1032=
ENST00000257430.9:c.3096A>T MANE Select	ENSP00000257430.4:p.Ser1032=
ENST00000257430.8:c.3096A>T	ENSP00000257430.4:p.Ser1032=
ENST00000502371.2:c.1449A>T
ENST00000507379.5:c.3042A>T	ENSP00000423224.1:p.Ser1014=
ENST00000508376.6:c.3096A>T	ENSP00000427089.2:p.Ser1032=
ENST00000508624.5:c.*2418A>T	ENSP00000424265.1:n.*2418A>T
ENST00000512211.6:c.3096A>T	ENSP00000423828.2:p.Ser1032=
ENST00000520401.1:c.230+9718A>T
NM_000038.5:c.3096A>T	NP_000029.2:p.Ser1032=
NM_001127510.2:c.3096A>T	NP_001120982.1:p.Ser1032=
NM_001127511.2:c.3042A>T	NP_001120983.2:p.Ser1014=
NM_001354895.1:c.3096A>T	NP_001341824.1:p.Ser1032=
NM_001354896.1:c.3150A>T	NP_001341825.1:p.Ser1050=
NM_001354897.1:c.3126A>T	NP_001341826.1:p.Ser1042=
NM_001354898.1:c.3021A>T	NP_001341827.1:p.Ser1007=
NM_001354899.1:c.3012A>T	NP_001341828.1:p.Ser1004=
NM_001354900.1:c.2973A>T	NP_001341829.1:p.Ser991=
NM_001354901.1:c.2919A>T	NP_001341830.1:p.Ser973=
NM_001354902.1:c.2823A>T	NP_001341831.1:p.Ser941=
NM_001354903.1:c.2793A>T	NP_001341832.1:p.Ser931=
NM_001354904.1:c.2718A>T	NP_001341833.1:p.Ser906=
NM_001354905.1:c.2616A>T	NP_001341834.1:p.Ser872=
NM_001354906.1:c.2247A>T	NP_001341835.1:p.Ser749=
NM_000038.6:c.3096A>T MANE Select	NP_000029.2:p.Ser1032=
NM_001127510.3:c.3096A>T	NP_001120982.1:p.Ser1032=
NM_001127511.3:c.3042A>T	NP_001120983.2:p.Ser1014=
NM_001354895.2:c.3096A>T	NP_001341824.1:p.Ser1032=
NM_001354896.2:c.3150A>T	NP_001341825.1:p.Ser1050=
NM_001354897.2:c.3126A>T	NP_001341826.1:p.Ser1042=
NM_001354898.2:c.3021A>T	NP_001341827.1:p.Ser1007=
NM_001354899.2:c.3012A>T	NP_001341828.1:p.Ser1004=
NM_001354900.2:c.2973A>T	NP_001341829.1:p.Ser991=
NM_001354901.2:c.2919A>T	NP_001341830.1:p.Ser973=
NM_001354902.2:c.2823A>T	NP_001341831.1:p.Ser941=
NM_001354903.2:c.2793A>T	NP_001341832.1:p.Ser931=
NM_001354904.2:c.2718A>T	NP_001341833.1:p.Ser906=
NM_001354905.2:c.2616A>T	NP_001341834.1:p.Ser872=
NM_001354906.2:c.2247A>T	NP_001341835.1:p.Ser749=