Canonical Allele Identifier: CA023459

Gene: APC

Linked Data

• ClinVar Variation Id: 82288
• ClinVar RCV Id: RCV000073277
• dbSNP Id: rs79707630
• MyVariant Identifiers: chr5:g.112063594G>T (hg19) ; chr5:g.112727897G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112727897G>T , CM000667.2:g.112727897G>T	GRCh38
NC_000005.9:g.112063594G>T , CM000667.1:g.112063594G>T	GRCh37
NC_000005.8:g.112091493G>T	NCBI36
NG_008481.4:g.40377G>T , LRG_130:g.40377G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000505350.2:c.165+20015G>T	ENSP00000481752.1:n.165+20015G>T
ENST00000507379.6:c.165+20015G>T	ENSP00000423224.2:n.165+20015G>T
ENST00000509732.6:c.-19+20248G>T	ENSP00000426541.2:n.-19+20248G>T
ENST00000505350.1:c.165+20015G>T	ENSP00000481752.1:n.165+20015G>T
ENST00000507379.5:c.165+20015G>T	ENSP00000423224.1:n.165+20015G>T
ENST00000509732.5:c.-19+20248G>T	ENSP00000426541.1:n.-19+20248G>T
NM_001127511.2:c.165+20015G>T	NP_001120983.2:n.165+20015G>T
NM_001354895.1:c.-19+20015G>T	NP_001341824.1:n.-19+20015G>T
NM_001354897.1:c.165+20015G>T	NP_001341826.1:n.165+20015G>T
NM_001354902.1:c.165+20015G>T	NP_001341831.1:n.165+20015G>T
NM_001127511.3:c.165+20015G>T	NP_001120983.2:n.165+20015G>T
NM_001354895.2:c.-19+20015G>T	NP_001341824.1:n.-19+20015G>T
NM_001354897.2:c.165+20015G>T	NP_001341826.1:n.165+20015G>T
NM_001354902.2:c.165+20015G>T	NP_001341831.1:n.165+20015G>T