Canonical Allele Identifier: CA1573442481

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707582G= , CM000667.2:g.112707582G=	GRCh38
NC_000005.9:g.112043279G= , CM000667.1:g.112043279G=	GRCh37
NC_000005.8:g.112071178G=	NCBI36
NG_008481.4:g.20062G= , LRG_130:g.20062G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-136G=	ENSP00000481752.1:n.-136G=
ENST00000507379.6:c.-136G=	ENSP00000423224.2:n.-136G=
ENST00000509732.6:c.-86G=	ENSP00000426541.2:n.-86G=
ENST00000505350.1:c.-136G=	ENSP00000481752.1:n.-136G=
ENST00000507379.5:c.-136G=	ENSP00000423224.1:n.-136G=
ENST00000509732.5:c.-86G=	ENSP00000426541.1:n.-86G=
NM_001127511.2:c.-136G=	NP_001120983.2:n.-136G=
NM_001354895.1:c.-319G=	NP_001341824.1:n.-319G=
NM_001354897.1:c.-136G=	NP_001341826.1:n.-136G=
NM_001354902.1:c.-136G=	NP_001341831.1:n.-136G=
NM_001127511.3:c.-136G=	NP_001120983.2:n.-136G=
NM_001354895.2:c.-319G=	NP_001341824.1:n.-319G=
NM_001354897.2:c.-136G=	NP_001341826.1:n.-136G=
NM_001354902.2:c.-136G=	NP_001341831.1:n.-136G=