Canonical Allele Identifier: CA2674864302

Gene: APC

Linked Data

• gnomAD v4: 5-112707925-T-TTCCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707926_112707930dup , CM000667.2:g.112707926_112707930dup	GRCh38
NC_000005.9:g.112043623_112043627dup , CM000667.1:g.112043623_112043627dup	GRCh37
NC_000005.8:g.112071522_112071526dup	NCBI36
NG_008481.4:g.20406_20410dup , LRG_130:g.20406_20410dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.165+44_165+48dup	ENSP00000481752.1:n.165+44_165+48dup
ENST00000507379.6:c.165+44_165+48dup	ENSP00000423224.2:n.165+44_165+48dup
ENST00000509732.6:c.-19+277_-19+281dup	ENSP00000426541.2:n.-19+277_-19+281dup
ENST00000505350.1:c.165+44_165+48dup	ENSP00000481752.1:n.165+44_165+48dup
ENST00000507379.5:c.165+44_165+48dup	ENSP00000423224.1:n.165+44_165+48dup
ENST00000509732.5:c.-19+277_-19+281dup	ENSP00000426541.1:n.-19+277_-19+281dup
NM_001127511.2:c.165+44_165+48dup	NP_001120983.2:n.165+44_165+48dup
NM_001354895.1:c.-19+44_-19+48dup	NP_001341824.1:n.-19+44_-19+48dup
NM_001354897.1:c.165+44_165+48dup	NP_001341826.1:n.165+44_165+48dup
NM_001354902.1:c.165+44_165+48dup	NP_001341831.1:n.165+44_165+48dup
NM_001127511.3:c.165+44_165+48dup	NP_001120983.2:n.165+44_165+48dup
NM_001354895.2:c.-19+44_-19+48dup	NP_001341824.1:n.-19+44_-19+48dup
NM_001354897.2:c.165+44_165+48dup	NP_001341826.1:n.165+44_165+48dup
NM_001354902.2:c.165+44_165+48dup	NP_001341831.1:n.165+44_165+48dup