Canonical Allele Identifier: CA304076379

Gene: APC2 C19orf25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1466156C>T , CM000681.2:g.1466156C>T	GRCh38
NC_000019.9:g.1466155C>T , CM000681.1:g.1466155C>T	GRCh37
NC_000019.8:g.1417155C>T	NCBI36
NG_055243.1:g.24889C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000590469.6:c.2855C>T (APC2) MANE Select	ENSP00000467073.2:p.Ser952Leu
ENST00000233607.6:c.2855C>T (APC2)	ENSP00000233607.2:p.Ser952Leu
ENST00000535453.5:c.2855C>T (APC2)	ENSP00000442954.1:p.Ser952Leu
ENST00000588427.5:c.131-4332G>A (C19orf25)	ENSP00000468000.1:n.131-4332G>A
NM_005883.2:c.2855C>T (APC2)	NP_005874.1:p.Ser952Leu
XM_005259475.2:c.2927C>T (APC2)	XP_005259532.1:p.Ser976Leu
XM_006722607.2:c.2924C>T (APC2)	XP_006722670.1:p.Ser975Leu
XM_006722608.2:c.2855C>T (APC2)	XP_006722671.1:p.Ser952Leu
XM_006722609.2:c.2855C>T (APC2)	XP_006722672.1:p.Ser952Leu
XM_006722610.2:c.2852C>T (APC2)	XP_006722673.1:p.Ser951Leu
NM_001351273.1:c.2852C>T (APC2)	NP_001338202.1:p.Ser951Leu
XM_006722608.3:c.3158C>T (APC2)	XP_006722671.2:p.Ser1053Leu
XM_006722609.3:c.2855C>T (APC2)	XP_006722672.1:p.Ser952Leu
XM_006722610.3:c.3155C>T (APC2)	XP_006722673.2:p.Ser1052Leu
NM_005883.3:c.2855C>T (APC2) MANE Select	NP_005874.1:p.Ser952Leu