Canonical Allele Identifier: CA124948565

Gene: APC

Linked Data

• dbSNP Id: rs916743523
• gnomAD v3: 5-112737552-C-T
• gnomAD v4: 5-112737552-C-T
• MyVariant Identifiers: chr5:g.112073249C>T (hg19) ; chr5:g.112737552C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112737552C>T , CM000667.2:g.112737552C>T	GRCh38
NC_000005.9:g.112073249C>T , CM000667.1:g.112073249C>T	GRCh37
NC_000005.8:g.112101148C>T	NCBI36
NG_008481.4:g.50032C>T , LRG_130:g.50032C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000505350.2:c.166-17321C>T	ENSP00000481752.1:n.166-17321C>T
ENST00000507379.6:c.166-28774C>T	ENSP00000423224.2:n.166-28774C>T
ENST00000509732.6:c.-18-17321C>T	ENSP00000426541.2:n.-18-17321C>T
ENST00000505350.1:c.166-17321C>T	ENSP00000481752.1:n.166-17321C>T
ENST00000507379.5:c.166-28774C>T	ENSP00000423224.1:n.166-28774C>T
ENST00000509732.5:c.-18-17321C>T	ENSP00000426541.1:n.-18-17321C>T
NM_001127511.2:c.166-28774C>T	NP_001120983.2:n.166-28774C>T
NM_001354895.1:c.-18-17321C>T	NP_001341824.1:n.-18-17321C>T
NM_001354897.1:c.166-28774C>T	NP_001341826.1:n.166-28774C>T
NM_001354902.1:c.166-28774C>T	NP_001341831.1:n.166-28774C>T
NM_001127511.3:c.166-28774C>T	NP_001120983.2:n.166-28774C>T
NM_001354895.2:c.-18-17321C>T	NP_001341824.1:n.-18-17321C>T
NM_001354897.2:c.166-28774C>T	NP_001341826.1:n.166-28774C>T
NM_001354902.2:c.166-28774C>T	NP_001341831.1:n.166-28774C>T