Canonical Allele Identifier: CA16042079

Gene: APC

Linked Data

• ClinVar Variation Id: 371917
• ClinVar RCV Id: RCV000410173 ; RCV002230742
• dbSNP Id: rs1057517584
• gnomAD v2: 5-112043536-C-T
• gnomAD v3: 5-112707839-C-T
• gnomAD v4: 5-112707839-C-T
• MyVariant Identifiers: chr5:g.112043536C>T (hg19) ; chr5:g.112707839C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707839C>T , CM000667.2:g.112707839C>T	GRCh38
NC_000005.9:g.112043536C>T , CM000667.1:g.112043536C>T	GRCh37
NC_000005.8:g.112071435C>T	NCBI36
NG_008481.4:g.20319C>T , LRG_130:g.20319C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.122C>T	ENSP00000481752.1:p.Pro41Leu
ENST00000507379.6:c.122C>T	ENSP00000423224.2:p.Pro41Leu
ENST00000509732.6:c.-19+190C>T	ENSP00000426541.2:n.-19+190C>T
ENST00000505350.1:c.122C>T	ENSP00000481752.1:p.Pro41Leu
ENST00000507379.5:c.122C>T	ENSP00000423224.1:p.Pro41Leu
ENST00000509732.5:c.-19+190C>T	ENSP00000426541.1:n.-19+190C>T
NM_001127511.2:c.122C>T	NP_001120983.2:p.Pro41Leu
NM_001354895.1:c.-62C>T	NP_001341824.1:n.-62C>T
NM_001354897.1:c.122C>T	NP_001341826.1:p.Pro41Leu
NM_001354902.1:c.122C>T	NP_001341831.1:p.Pro41Leu
NM_001127511.3:c.122C>T	NP_001120983.2:p.Pro41Leu
NM_001354895.2:c.-62C>T	NP_001341824.1:n.-62C>T
NM_001354897.2:c.122C>T	NP_001341826.1:p.Pro41Leu
NM_001354902.2:c.122C>T	NP_001341831.1:p.Pro41Leu