Canonical Allele Identifier: CA2674863525

Gene: APC

Linked Data

• gnomAD v4: 5-112707559-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707561del , CM000667.2:g.112707561del	GRCh38
NC_000005.9:g.112043258del , CM000667.1:g.112043258del	GRCh37
NC_000005.8:g.112071157del	NCBI36
NG_008481.4:g.20041del , LRG_130:g.20041del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-157del	ENSP00000481752.1:n.-157del
ENST00000507379.6:c.-157del	ENSP00000423224.2:n.-157del
ENST00000509732.6:c.-107del	ENSP00000426541.2:n.-107del
ENST00000505350.1:c.-157del	ENSP00000481752.1:n.-157del
ENST00000507379.5:c.-157del	ENSP00000423224.1:n.-157del
ENST00000509732.5:c.-107del	ENSP00000426541.1:n.-107del
NM_001127511.2:c.-157del	NP_001120983.2:n.-157del
NM_001354895.1:c.-340del	NP_001341824.1:n.-340del
NM_001354897.1:c.-157del	NP_001341826.1:n.-157del
NM_001354902.1:c.-157del	NP_001341831.1:n.-157del
NM_001127511.3:c.-157del	NP_001120983.2:n.-157del
NM_001354895.2:c.-340del	NP_001341824.1:n.-340del
NM_001354897.2:c.-157del	NP_001341826.1:n.-157del
NM_001354902.2:c.-157del	NP_001341831.1:n.-157del