Canonical Allele Identifier: CA1573442406

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707536G= , CM000667.2:g.112707536G=	GRCh38
NC_000005.9:g.112043233G= , CM000667.1:g.112043233G=	GRCh37
NC_000005.8:g.112071132G=	NCBI36
NG_008481.4:g.20016G= , LRG_130:g.20016G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-182G=	ENSP00000481752.1:n.-182G=
ENST00000507379.6:c.-182G=	ENSP00000423224.2:n.-182G=
ENST00000509732.6:c.-132G=	ENSP00000426541.2:n.-132G=
ENST00000505350.1:c.-182G=	ENSP00000481752.1:n.-182G=
ENST00000507379.5:c.-182G=	ENSP00000423224.1:n.-182G=
ENST00000509732.5:c.-132G=	ENSP00000426541.1:n.-132G=
NM_001127511.2:c.-182G=	NP_001120983.2:n.-182G=
NM_001354895.1:c.-365G=	NP_001341824.1:n.-365G=
NM_001354897.1:c.-182G=	NP_001341826.1:n.-182G=
NM_001354902.1:c.-182G=	NP_001341831.1:n.-182G=
NM_001127511.3:c.-182G=	NP_001120983.2:n.-182G=
NM_001354895.2:c.-365G=	NP_001341824.1:n.-365G=
NM_001354897.2:c.-182G=	NP_001341826.1:n.-182G=
NM_001354902.2:c.-182G=	NP_001341831.1:n.-182G=