Canonical Allele Identifier: CA9044931

Gene: APC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1456952G>A , CM000681.2:g.1456952G>A	GRCh38
NC_000019.9:g.1456951G>A , CM000681.1:g.1456951G>A	GRCh37
NC_000019.8:g.1407951G>A	NCBI36
NG_055243.1:g.15685G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005883.3:c.916G>A MANE Select	NP_005874.1:p.Val306Met
ENST00000590469.6:c.916G>A MANE Select	ENSP00000467073.2:p.Val306Met
NM_001351273.1:c.913G>A	NP_001338202.1:p.Val305Met
NM_005883.2:c.916G>A	NP_005874.1:p.Val306Met
ENST00000233607.6:c.916G>A	ENSP00000233607.2:p.Val306Met
ENST00000238483.5:c.913G>A	ENSP00000238483.5:p.Val305Met
ENST00000535453.5:c.916G>A	ENSP00000442954.1:p.Val306Met
ENST00000590469.5:c.916G>A	ENSP00000467073.1:p.Val306Met
ENST00000593146.1:n.975G>A
XM_005259475.2:c.988G>A	XP_005259532.1:p.Val330Met
XM_006722607.2:c.985G>A	XP_006722670.1:p.Val329Met
XM_006722608.2:c.916G>A	XP_006722671.1:p.Val306Met
XM_006722608.3:c.1219G>A	XP_006722671.2:p.Val407Met
XM_006722609.2:c.916G>A	XP_006722672.1:p.Val306Met
XM_006722609.3:c.916G>A	XP_006722672.1:p.Val306Met
XM_006722610.2:c.913G>A	XP_006722673.1:p.Val305Met
XM_006722610.3:c.1216G>A	XP_006722673.2:p.Val406Met