Canonical Allele Identifier: CA403014451

Gene: APC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1456913C>T , CM000681.2:g.1456913C>T	GRCh38
NC_000019.9:g.1456912C>T , CM000681.1:g.1456912C>T	GRCh37
NC_000019.8:g.1407912C>T	NCBI36
NG_055243.1:g.15646C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000590469.6:c.877C>T MANE Select	ENSP00000467073.2:p.Arg293Cys
ENST00000233607.6:c.877C>T	ENSP00000233607.2:p.Arg293Cys
ENST00000238483.5:c.874C>T	ENSP00000238483.5:p.Arg292Cys
ENST00000535453.5:c.877C>T	ENSP00000442954.1:p.Arg293Cys
ENST00000590469.5:c.877C>T	ENSP00000467073.1:p.Arg293Cys
ENST00000593146.1:n.936C>T
NM_005883.2:c.877C>T	NP_005874.1:p.Arg293Cys
XM_005259475.2:c.949C>T	XP_005259532.1:p.Arg317Cys
XM_006722607.2:c.946C>T	XP_006722670.1:p.Arg316Cys
XM_006722608.2:c.877C>T	XP_006722671.1:p.Arg293Cys
XM_006722609.2:c.877C>T	XP_006722672.1:p.Arg293Cys
XM_006722610.2:c.874C>T	XP_006722673.1:p.Arg292Cys
NM_001351273.1:c.874C>T	NP_001338202.1:p.Arg292Cys
XM_006722608.3:c.1180C>T	XP_006722671.2:p.Arg394Cys
XM_006722609.3:c.877C>T	XP_006722672.1:p.Arg293Cys
XM_006722610.3:c.1177C>T	XP_006722673.2:p.Arg393Cys
NM_005883.3:c.877C>T MANE Select	NP_005874.1:p.Arg293Cys