Canonical Allele Identifier: CA802057396

Gene: APC

Linked Data

• dbSNP Id: rs1379945489
• MyVariant Identifiers: chr5:g.112043471_112043477del (hg19) ; chr5:g.112707774_112707780del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707777_112707783del , CM000667.2:g.112707777_112707783del	GRCh38
NC_000005.9:g.112043474_112043480del , CM000667.1:g.112043474_112043480del	GRCh37
NC_000005.8:g.112071373_112071379del	NCBI36
NG_008481.4:g.20257_20263del , LRG_130:g.20257_20263del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.60_66del	ENSP00000481752.1:p.Val21GlyfsTer?
ENST00000507379.6:c.60_66del	ENSP00000423224.2:p.Val21GlyfsTer?
ENST00000509732.6:c.-19+128_-19+134del	ENSP00000426541.2:n.-19+128_-19+134del
ENST00000505350.1:c.60_66del	ENSP00000481752.1:p.Val21GlyfsTer?
ENST00000507379.5:c.60_66del	ENSP00000423224.1:p.Val21GlyfsTer?
ENST00000509732.5:c.-19+128_-19+134del	ENSP00000426541.1:n.-19+128_-19+134del
NM_001127511.2:c.60_66del	NP_001120983.2:p.Val21GlyfsTer?
NM_001354895.1:c.-124_-118del	NP_001341824.1:n.-124_-118del
NM_001354897.1:c.60_66del	NP_001341826.1:p.Val21GlyfsTer?
NM_001354902.1:c.60_66del	NP_001341831.1:p.Val21GlyfsTer?
NM_001127511.3:c.60_66del	NP_001120983.2:p.Val21GlyfsTer?
NM_001354895.2:c.-124_-118del	NP_001341824.1:n.-124_-118del
NM_001354897.2:c.60_66del	NP_001341826.1:p.Val21GlyfsTer?
NM_001354902.2:c.60_66del	NP_001341831.1:p.Val21GlyfsTer?