Canonical Allele Identifier: CA360611832

Gene: APC

Linked Data

• ClinVar Variation Id: 1041235
• ClinVar RCV Id: RCV002547025
• dbSNP Id: rs1750607611
• gnomAD v4: 5-112707782-T-C
• MyVariant Identifiers: chr5:g.112043479T>C (hg19) ; chr5:g.112707782T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707782T>C , CM000667.2:g.112707782T>C	GRCh38
NC_000005.9:g.112043479T>C , CM000667.1:g.112043479T>C	GRCh37
NC_000005.8:g.112071378T>C	NCBI36
NG_008481.4:g.20262T>C , LRG_130:g.20262T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.65T>C	ENSP00000481752.1:p.Leu22Pro
ENST00000507379.6:c.65T>C	ENSP00000423224.2:p.Leu22Pro
ENST00000509732.6:c.-19+133T>C	ENSP00000426541.2:n.-19+133T>C
ENST00000505350.1:c.65T>C	ENSP00000481752.1:p.Leu22Pro
ENST00000507379.5:c.65T>C	ENSP00000423224.1:p.Leu22Pro
ENST00000509732.5:c.-19+133T>C	ENSP00000426541.1:n.-19+133T>C
NM_001127511.2:c.65T>C	NP_001120983.2:p.Leu22Pro
NM_001354895.1:c.-119T>C	NP_001341824.1:n.-119T>C
NM_001354897.1:c.65T>C	NP_001341826.1:p.Leu22Pro
NM_001354902.1:c.65T>C	NP_001341831.1:p.Leu22Pro
NM_001127511.3:c.65T>C	NP_001120983.2:p.Leu22Pro
NM_001354895.2:c.-119T>C	NP_001341824.1:n.-119T>C
NM_001354897.2:c.65T>C	NP_001341826.1:p.Leu22Pro
NM_001354902.2:c.65T>C	NP_001341831.1:p.Leu22Pro