Canonical Allele Identifier: CA124924922

Gene: APC

Linked Data

• ClinVar Variation Id: 1062295
• ClinVar RCV Id: RCV003538761
• dbSNP Id: rs982566204
• gnomAD v2: 5-112043279-G-C
• gnomAD v3: 5-112707582-G-C
• gnomAD v4: 5-112707582-G-C
• MyVariant Identifiers: chr5:g.112043279G>C (hg19) ; chr5:g.112707582G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707582G>C , CM000667.2:g.112707582G>C	GRCh38
NC_000005.9:g.112043279G>C , CM000667.1:g.112043279G>C	GRCh37
NC_000005.8:g.112071178G>C	NCBI36
NG_008481.4:g.20062G>C , LRG_130:g.20062G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-136G>C	ENSP00000481752.1:n.-136G>C
ENST00000507379.6:c.-136G>C	ENSP00000423224.2:n.-136G>C
ENST00000509732.6:c.-86G>C	ENSP00000426541.2:n.-86G>C
ENST00000505350.1:c.-136G>C	ENSP00000481752.1:n.-136G>C
ENST00000507379.5:c.-136G>C	ENSP00000423224.1:n.-136G>C
ENST00000509732.5:c.-86G>C	ENSP00000426541.1:n.-86G>C
NM_001127511.2:c.-136G>C	NP_001120983.2:n.-136G>C
NM_001354895.1:c.-319G>C	NP_001341824.1:n.-319G>C
NM_001354897.1:c.-136G>C	NP_001341826.1:n.-136G>C
NM_001354902.1:c.-136G>C	NP_001341831.1:n.-136G>C
NM_001127511.3:c.-136G>C	NP_001120983.2:n.-136G>C
NM_001354895.2:c.-319G>C	NP_001341824.1:n.-319G>C
NM_001354897.2:c.-136G>C	NP_001341826.1:n.-136G>C
NM_001354902.2:c.-136G>C	NP_001341831.1:n.-136G>C