Canonical Allele Identifier: CA2578379454

Gene: APC

Linked Data

• gnomAD v4: 5-112707922-AGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707923_112707924del , CM000667.2:g.112707923_112707924del	GRCh38
NC_000005.9:g.112043620_112043621del , CM000667.1:g.112043620_112043621del	GRCh37
NC_000005.8:g.112071519_112071520del	NCBI36
NG_008481.4:g.20403_20404del , LRG_130:g.20403_20404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.165+41_165+42del	ENSP00000481752.1:n.165+41_165+42del
ENST00000507379.6:c.165+41_165+42del	ENSP00000423224.2:n.165+41_165+42del
ENST00000509732.6:c.-19+274_-19+275del	ENSP00000426541.2:n.-19+274_-19+275del
ENST00000505350.1:c.165+41_165+42del	ENSP00000481752.1:n.165+41_165+42del
ENST00000507379.5:c.165+41_165+42del	ENSP00000423224.1:n.165+41_165+42del
ENST00000509732.5:c.-19+274_-19+275del	ENSP00000426541.1:n.-19+274_-19+275del
NM_001127511.2:c.165+41_165+42del	NP_001120983.2:n.165+41_165+42del
NM_001354895.1:c.-19+41_-19+42del	NP_001341824.1:n.-19+41_-19+42del
NM_001354897.1:c.165+41_165+42del	NP_001341826.1:n.165+41_165+42del
NM_001354902.1:c.165+41_165+42del	NP_001341831.1:n.165+41_165+42del
NM_001127511.3:c.165+41_165+42del	NP_001120983.2:n.165+41_165+42del
NM_001354895.2:c.-19+41_-19+42del	NP_001341824.1:n.-19+41_-19+42del
NM_001354897.2:c.165+41_165+42del	NP_001341826.1:n.165+41_165+42del
NM_001354902.2:c.165+41_165+42del	NP_001341831.1:n.165+41_165+42del