Canonical Allele Identifier: CA2580072326

Gene: APC

Linked Data

• ClinVar Variation Id: 2116738
• ClinVar RCV Id: RCV003744955
• dbSNP Id: rs1750604976

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707750C>T , CM000667.2:g.112707750C>T	GRCh38
NC_000005.9:g.112043447C>T , CM000667.1:g.112043447C>T	GRCh37
NC_000005.8:g.112071346C>T	NCBI36
NG_008481.4:g.20230C>T , LRG_130:g.20230C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.33C>T	ENSP00000481752.1:p.Ala11=
ENST00000507379.6:c.33C>T	ENSP00000423224.2:p.Ala11=
ENST00000509732.6:c.-19+101C>T	ENSP00000426541.2:n.-19+101C>T
ENST00000505350.1:c.33C>T	ENSP00000481752.1:p.Ala11=
ENST00000507379.5:c.33C>T	ENSP00000423224.1:p.Ala11=
ENST00000509732.5:c.-19+101C>T	ENSP00000426541.1:n.-19+101C>T
NM_001127511.2:c.33C>T	NP_001120983.2:p.Ala11=
NM_001354895.1:c.-151C>T	NP_001341824.1:n.-151C>T
NM_001354897.1:c.33C>T	NP_001341826.1:p.Ala11=
NM_001354902.1:c.33C>T	NP_001341831.1:p.Ala11=
NM_001127511.3:c.33C>T	NP_001120983.2:p.Ala11=
NM_001354895.2:c.-151C>T	NP_001341824.1:n.-151C>T
NM_001354897.2:c.33C>T	NP_001341826.1:p.Ala11=
NM_001354902.2:c.33C>T	NP_001341831.1:p.Ala11=