Canonical Allele Identifier: CA403022128

Gene: APC2 C19orf25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1462115C>G , CM000681.2:g.1462115C>G	GRCh38
NC_000019.9:g.1462114C>G , CM000681.1:g.1462114C>G	GRCh37
NC_000019.8:g.1413114C>G	NCBI36
NG_055243.1:g.20848C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005883.3:c.1791C>G (APC2) MANE Select	NP_005874.1:p.Ile597Met
ENST00000590469.6:c.1791C>G (APC2) MANE Select	ENSP00000467073.2:p.Ile597Met
NM_001351273.1:c.1788C>G (APC2)	NP_001338202.1:p.Ile596Met
NM_005883.2:c.1791C>G (APC2)	NP_005874.1:p.Ile597Met
ENST00000233607.6:c.1791C>G (APC2)	ENSP00000233607.2:p.Ile597Met
ENST00000238483.5:c.1788C>G (APC2)	ENSP00000238483.5:p.Ile596Met
ENST00000535453.5:c.1791C>G (APC2)	ENSP00000442954.1:p.Ile597Met
ENST00000588427.5:c.131-291G>C (C19orf25)	ENSP00000468000.1:n.131-291G>C
ENST00000590469.5:c.1791C>G (APC2)	ENSP00000467073.1:p.Ile597Met
ENST00000593146.1:n.2571C>G (APC2)
XM_005259475.2:c.1863C>G (APC2)	XP_005259532.1:p.Ile621Met
XM_006722607.2:c.1860C>G (APC2)	XP_006722670.1:p.Ile620Met
XM_006722608.2:c.1791C>G (APC2)	XP_006722671.1:p.Ile597Met
XM_006722608.3:c.2094C>G (APC2)	XP_006722671.2:p.Ile698Met
XM_006722609.2:c.1791C>G (APC2)	XP_006722672.1:p.Ile597Met
XM_006722609.3:c.1791C>G (APC2)	XP_006722672.1:p.Ile597Met
XM_006722610.2:c.1788C>G (APC2)	XP_006722673.1:p.Ile596Met
XM_006722610.3:c.2091C>G (APC2)	XP_006722673.2:p.Ile697Met