Canonical Allele Identifier: CA2674863502

Gene: APC

Linked Data

• gnomAD v4: 5-112707529-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707529G>T , CM000667.2:g.112707529G>T	GRCh38
NC_000005.9:g.112043226G>T , CM000667.1:g.112043226G>T	GRCh37
NC_000005.8:g.112071125G>T	NCBI36
NG_008481.4:g.20009G>T , LRG_130:g.20009G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-189G>T	ENSP00000481752.1:n.-189G>T
ENST00000507379.6:c.-189G>T	ENSP00000423224.2:n.-189G>T
ENST00000509732.6:c.-139G>T	ENSP00000426541.2:n.-139G>T
ENST00000505350.1:c.-189G>T	ENSP00000481752.1:n.-189G>T
ENST00000507379.5:c.-189G>T	ENSP00000423224.1:n.-189G>T
ENST00000509732.5:c.-139G>T	ENSP00000426541.1:n.-139G>T
NM_001127511.2:c.-189G>T	NP_001120983.2:n.-189G>T
NM_001354895.1:c.-372G>T	NP_001341824.1:n.-372G>T
NM_001354897.1:c.-189G>T	NP_001341826.1:n.-189G>T
NM_001354902.1:c.-189G>T	NP_001341831.1:n.-189G>T
NM_001127511.3:c.-189G>T	NP_001120983.2:n.-189G>T
NM_001354895.2:c.-372G>T	NP_001341824.1:n.-372G>T
NM_001354897.2:c.-189G>T	NP_001341826.1:n.-189G>T
NM_001354902.2:c.-189G>T	NP_001341831.1:n.-189G>T