Canonical Allele Identifier: CA2674863572

Gene: APC

Linked Data

• ClinVar Variation Id: 2725811
• ClinVar RCV Id: RCV003538954
• gnomAD v4: 5-112707620-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707620G>T , CM000667.2:g.112707620G>T	GRCh38
NC_000005.9:g.112043317G>T , CM000667.1:g.112043317G>T	GRCh37
NC_000005.8:g.112071216G>T	NCBI36
NG_008481.4:g.20100G>T , LRG_130:g.20100G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-98G>T	ENSP00000481752.1:n.-98G>T
ENST00000507379.6:c.-98G>T	ENSP00000423224.2:n.-98G>T
ENST00000509732.6:c.-48G>T	ENSP00000426541.2:n.-48G>T
ENST00000505350.1:c.-98G>T	ENSP00000481752.1:n.-98G>T
ENST00000507379.5:c.-98G>T	ENSP00000423224.1:n.-98G>T
ENST00000509732.5:c.-48G>T	ENSP00000426541.1:n.-48G>T
NM_001127511.2:c.-98G>T	NP_001120983.2:n.-98G>T
NM_001354895.1:c.-281G>T	NP_001341824.1:n.-281G>T
NM_001354897.1:c.-98G>T	NP_001341826.1:n.-98G>T
NM_001354902.1:c.-98G>T	NP_001341831.1:n.-98G>T
NM_001127511.3:c.-98G>T	NP_001120983.2:n.-98G>T
NM_001354895.2:c.-281G>T	NP_001341824.1:n.-281G>T
NM_001354897.2:c.-98G>T	NP_001341826.1:n.-98G>T
NM_001354902.2:c.-98G>T	NP_001341831.1:n.-98G>T