Canonical Allele Identifier: CA9044885

Gene: APC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1456384C>T , CM000681.2:g.1456384C>T	GRCh38
NC_000019.9:g.1456383C>T , CM000681.1:g.1456383C>T	GRCh37
NC_000019.8:g.1407383C>T	NCBI36
NG_055243.1:g.15117C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005883.3:c.796C>T MANE Select	NP_005874.1:p.Pro266Ser
ENST00000590469.6:c.796C>T MANE Select	ENSP00000467073.2:p.Pro266Ser
NM_001351273.1:c.793C>T	NP_001338202.1:p.Pro265Ser
NM_005883.2:c.796C>T	NP_005874.1:p.Pro266Ser
ENST00000233607.6:c.796C>T	ENSP00000233607.2:p.Pro266Ser
ENST00000238483.5:c.793C>T	ENSP00000238483.5:p.Pro265Ser
ENST00000535453.5:c.796C>T	ENSP00000442954.1:p.Pro266Ser
ENST00000590469.5:c.796C>T	ENSP00000467073.1:p.Pro266Ser
ENST00000593146.1:n.855C>T
XM_005259475.2:c.868C>T	XP_005259532.1:p.Pro290Ser
XM_006722607.2:c.865C>T	XP_006722670.1:p.Pro289Ser
XM_006722608.2:c.796C>T	XP_006722671.1:p.Pro266Ser
XM_006722608.3:c.1099C>T	XP_006722671.2:p.Pro367Ser
XM_006722609.2:c.796C>T	XP_006722672.1:p.Pro266Ser
XM_006722609.3:c.796C>T	XP_006722672.1:p.Pro266Ser
XM_006722610.2:c.793C>T	XP_006722673.1:p.Pro265Ser
XM_006722610.3:c.1096C>T	XP_006722673.2:p.Pro366Ser