Canonical Allele Identifier: CA2580072330

Gene: APC

Linked Data

• ClinVar Variation Id: 1992968
• ClinVar RCV Id: RCV003742866

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707798del , CM000667.2:g.112707798del	GRCh38
NC_000005.9:g.112043495del , CM000667.1:g.112043495del	GRCh37
NC_000005.8:g.112071394del	NCBI36
NG_008481.4:g.20278del , LRG_130:g.20278del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.81del	ENSP00000481752.1:p.Gly28AlafsTer?
ENST00000507379.6:c.81del	ENSP00000423224.2:p.Gly28AlafsTer?
ENST00000509732.6:c.-19+149del	ENSP00000426541.2:n.-19+149del
ENST00000505350.1:c.81del	ENSP00000481752.1:p.Gly28AlafsTer?
ENST00000507379.5:c.81del	ENSP00000423224.1:p.Gly28AlafsTer?
ENST00000509732.5:c.-19+149del	ENSP00000426541.1:n.-19+149del
NM_001127511.2:c.81del	NP_001120983.2:p.Gly28AlafsTer?
NM_001354895.1:c.-103del	NP_001341824.1:n.-103del
NM_001354897.1:c.81del	NP_001341826.1:p.Gly28AlafsTer?
NM_001354902.1:c.81del	NP_001341831.1:p.Gly28AlafsTer?
NM_001127511.3:c.81del	NP_001120983.2:p.Gly28AlafsTer?
NM_001354895.2:c.-103del	NP_001341824.1:n.-103del
NM_001354897.2:c.81del	NP_001341826.1:p.Gly28AlafsTer?
NM_001354902.2:c.81del	NP_001341831.1:p.Gly28AlafsTer?