Canonical Allele Identifier: CA9046126

Gene: APC2 C19orf25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1469372C>T , CM000681.2:g.1469372C>T	GRCh38
NC_000019.9:g.1469371C>T , CM000681.1:g.1469371C>T	GRCh37
NC_000019.8:g.1420371C>T	NCBI36
NG_055243.1:g.28105C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005883.3:c.6071C>T (APC2) MANE Select	NP_005874.1:p.Ala2024Val
ENST00000590469.6:c.6071C>T (APC2) MANE Select	ENSP00000467073.2:p.Ala2024Val
NM_001351273.1:c.6068C>T (APC2)	NP_001338202.1:p.Ala2023Val
NM_005883.2:c.6071C>T (APC2)	NP_005874.1:p.Ala2024Val
ENST00000233607.6:c.6071C>T (APC2)	ENSP00000233607.2:p.Ala2024Val
ENST00000535453.5:c.6071C>T (APC2)	ENSP00000442954.1:p.Ala2024Val
ENST00000588427.5:c.131-7548G>A (C19orf25)	ENSP00000468000.1:n.131-7548G>A
XM_005259475.2:c.6143C>T (APC2)	XP_005259532.1:p.Ala2048Val
XM_006722607.2:c.6140C>T (APC2)	XP_006722670.1:p.Ala2047Val
XM_006722608.2:c.6071C>T (APC2)	XP_006722671.1:p.Ala2024Val
XM_006722608.3:c.6374C>T (APC2)	XP_006722671.2:p.Ala2125Val
XM_006722609.2:c.6071C>T (APC2)	XP_006722672.1:p.Ala2024Val
XM_006722609.3:c.6071C>T (APC2)	XP_006722672.1:p.Ala2024Val
XM_006722610.2:c.6068C>T (APC2)	XP_006722673.1:p.Ala2023Val
XM_006722610.3:c.6371C>T (APC2)	XP_006722673.2:p.Ala2124Val