Canonical Allele Identifier: CA1573442479

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707581T= , CM000667.2:g.112707581T=	GRCh38
NC_000005.9:g.112043278T= , CM000667.1:g.112043278T=	GRCh37
NC_000005.8:g.112071177T=	NCBI36
NG_008481.4:g.20061T= , LRG_130:g.20061T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-137T=	ENSP00000481752.1:n.-137T=
ENST00000507379.6:c.-137T=	ENSP00000423224.2:n.-137T=
ENST00000509732.6:c.-87T=	ENSP00000426541.2:n.-87T=
ENST00000505350.1:c.-137T=	ENSP00000481752.1:n.-137T=
ENST00000507379.5:c.-137T=	ENSP00000423224.1:n.-137T=
ENST00000509732.5:c.-87T=	ENSP00000426541.1:n.-87T=
NM_001127511.2:c.-137T=	NP_001120983.2:n.-137T=
NM_001354895.1:c.-320T=	NP_001341824.1:n.-320T=
NM_001354897.1:c.-137T=	NP_001341826.1:n.-137T=
NM_001354902.1:c.-137T=	NP_001341831.1:n.-137T=
NM_001127511.3:c.-137T=	NP_001120983.2:n.-137T=
NM_001354895.2:c.-320T=	NP_001341824.1:n.-320T=
NM_001354897.2:c.-137T=	NP_001341826.1:n.-137T=
NM_001354902.2:c.-137T=	NP_001341831.1:n.-137T=