Canonical Allele Identifier: CA2580072333

Gene: APC

Linked Data

• ClinVar Variation Id: 2093937
• ClinVar RCV Id: RCV003744874

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707803del , CM000667.2:g.112707803del	GRCh38
NC_000005.9:g.112043500del , CM000667.1:g.112043500del	GRCh37
NC_000005.8:g.112071399del	NCBI36
NG_008481.4:g.20283del , LRG_130:g.20283del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.86del	ENSP00000481752.1:p.Gly29AlafsTer?
ENST00000507379.6:c.86del	ENSP00000423224.2:p.Gly29AlafsTer?
ENST00000509732.6:c.-19+154del	ENSP00000426541.2:n.-19+154del
ENST00000505350.1:c.86del	ENSP00000481752.1:p.Gly29AlafsTer?
ENST00000507379.5:c.86del	ENSP00000423224.1:p.Gly29AlafsTer?
ENST00000509732.5:c.-19+154del	ENSP00000426541.1:n.-19+154del
NM_001127511.2:c.86del	NP_001120983.2:p.Gly29AlafsTer?
NM_001354895.1:c.-98del	NP_001341824.1:n.-98del
NM_001354897.1:c.86del	NP_001341826.1:p.Gly29AlafsTer?
NM_001354902.1:c.86del	NP_001341831.1:p.Gly29AlafsTer?
NM_001127511.3:c.86del	NP_001120983.2:p.Gly29AlafsTer?
NM_001354895.2:c.-98del	NP_001341824.1:n.-98del
NM_001354897.2:c.86del	NP_001341826.1:p.Gly29AlafsTer?
NM_001354902.2:c.86del	NP_001341831.1:p.Gly29AlafsTer?