Canonical Allele Identifier: CA16038046

Gene: APC

Linked Data

• dbSNP Id: rs2149992067
• MyVariant Identifiers: chr5:g.112178986A>T (hg19) ; chr5:g.112843289A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843289A>T , CM000667.2:g.112843289A>T	GRCh38
NC_000005.9:g.112178986A>T , CM000667.1:g.112178986A>T	GRCh37
NC_000005.8:g.112206885A>T	NCBI36
NG_008481.4:g.155769A>T , LRG_130:g.155769A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7749A>T	ENSP00000473355.2:p.Arg2583Ser
ENST00000505350.2:c.*7701A>T	ENSP00000481752.1:n.*7701A>T
ENST00000507379.6:c.7641A>T	ENSP00000423224.2:p.Arg2547Ser
ENST00000509732.6:c.7695A>T	ENSP00000426541.2:p.Arg2565Ser
ENST00000512211.7:c.7695A>T	ENSP00000423828.3:p.Arg2565Ser
ENST00000257430.9:c.7695A>T MANE Select	ENSP00000257430.4:p.Arg2565Ser
ENST00000257430.8:c.7695A>T	ENSP00000257430.4:p.Arg2565Ser
ENST00000508376.6:c.7695A>T	ENSP00000427089.2:p.Arg2565Ser
ENST00000520401.1:c.231-13360A>T
NM_000038.5:c.7695A>T	NP_000029.2:p.Arg2565Ser
NM_001127510.2:c.7695A>T	NP_001120982.1:p.Arg2565Ser
NM_001127511.2:c.7641A>T	NP_001120983.2:p.Arg2547Ser
NM_001354895.1:c.7695A>T	NP_001341824.1:p.Arg2565Ser
NM_001354896.1:c.7749A>T	NP_001341825.1:p.Arg2583Ser
NM_001354897.1:c.7725A>T	NP_001341826.1:p.Arg2575Ser
NM_001354898.1:c.7620A>T	NP_001341827.1:p.Arg2540Ser
NM_001354899.1:c.7611A>T	NP_001341828.1:p.Arg2537Ser
NM_001354900.1:c.7572A>T	NP_001341829.1:p.Arg2524Ser
NM_001354901.1:c.7518A>T	NP_001341830.1:p.Arg2506Ser
NM_001354902.1:c.7422A>T	NP_001341831.1:p.Arg2474Ser
NM_001354903.1:c.7392A>T	NP_001341832.1:p.Arg2464Ser
NM_001354904.1:c.7317A>T	NP_001341833.1:p.Arg2439Ser
NM_001354905.1:c.7215A>T	NP_001341834.1:p.Arg2405Ser
NM_001354906.1:c.6846A>T	NP_001341835.1:p.Arg2282Ser
NM_000038.6:c.7695A>T MANE Select	NP_000029.2:p.Arg2565Ser
NM_001127510.3:c.7695A>T	NP_001120982.1:p.Arg2565Ser
NM_001127511.3:c.7641A>T	NP_001120983.2:p.Arg2547Ser
NM_001354895.2:c.7695A>T	NP_001341824.1:p.Arg2565Ser
NM_001354896.2:c.7749A>T	NP_001341825.1:p.Arg2583Ser
NM_001354897.2:c.7725A>T	NP_001341826.1:p.Arg2575Ser
NM_001354898.2:c.7620A>T	NP_001341827.1:p.Arg2540Ser
NM_001354899.2:c.7611A>T	NP_001341828.1:p.Arg2537Ser
NM_001354900.2:c.7572A>T	NP_001341829.1:p.Arg2524Ser
NM_001354901.2:c.7518A>T	NP_001341830.1:p.Arg2506Ser
NM_001354902.2:c.7422A>T	NP_001341831.1:p.Arg2474Ser
NM_001354903.2:c.7392A>T	NP_001341832.1:p.Arg2464Ser
NM_001354904.2:c.7317A>T	NP_001341833.1:p.Arg2439Ser
NM_001354905.2:c.7215A>T	NP_001341834.1:p.Arg2405Ser
NM_001354906.2:c.6846A>T	NP_001341835.1:p.Arg2282Ser