Canonical Allele Identifier: CA1080209712

Gene: APC

Linked Data

• gnomAD v3: 5-112727949-TAA-T
• gnomAD v4: 5-112727949-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112727959_112727960del , CM000667.2:g.112727959_112727960del	GRCh38
NC_000005.9:g.112063656_112063657del , CM000667.1:g.112063656_112063657del	GRCh37
NC_000005.8:g.112091555_112091556del	NCBI36
NG_008481.4:g.40439_40440del , LRG_130:g.40439_40440del

Transcript Alleles

HGVS	Amino-acid change
ENST00000505350.2:c.165+20077_165+20078del	ENSP00000481752.1:n.165+20077_165+20078de...
ENST00000507379.6:c.165+20077_165+20078del	ENSP00000423224.2:n.165+20077_165+20078de...
ENST00000509732.6:c.-19+20310_-19+20311del	ENSP00000426541.2:n.-19+20310_-19+20311de...
ENST00000505350.1:c.165+20077_165+20078del	ENSP00000481752.1:n.165+20077_165+20078de...
ENST00000507379.5:c.165+20077_165+20078del	ENSP00000423224.1:n.165+20077_165+20078de...
ENST00000509732.5:c.-19+20310_-19+20311del	ENSP00000426541.1:n.-19+20310_-19+20311de...
NM_001127511.2:c.165+20077_165+20078del	NP_001120983.2:n.165+20077_165+20078del
NM_001354895.1:c.-19+20077_-19+20078del	NP_001341824.1:n.-19+20077_-19+20078del
NM_001354897.1:c.165+20077_165+20078del	NP_001341826.1:n.165+20077_165+20078del
NM_001354902.1:c.165+20077_165+20078del	NP_001341831.1:n.165+20077_165+20078del
NM_001127511.3:c.165+20077_165+20078del	NP_001120983.2:n.165+20077_165+20078del
NM_001354895.2:c.-19+20077_-19+20078del	NP_001341824.1:n.-19+20077_-19+20078del
NM_001354897.2:c.165+20077_165+20078del	NP_001341826.1:n.165+20077_165+20078del
NM_001354902.2:c.165+20077_165+20078del	NP_001341831.1:n.165+20077_165+20078del