Canonical Allele Identifier: CA2369030926

Gene: NFATC2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51524725T= , CM000682.2:g.51524725T=	GRCh38
NC_000020.10:g.50141264T= , CM000682.1:g.50141264T=	GRCh37
NC_000020.9:g.49574671T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_012340.5:c.131-615A= MANE Select	NP_036472.2:n.131-615A=
ENST00000371564.8:c.131-615A= MANE Select	ENSP00000360619.3:n.131-615A=
NM_001136021.2:c.71-615A=	NP_001129493.1:n.71-615A=
NM_001136021.3:c.71-615A=	NP_001129493.1:n.71-615A=
NM_001258292.1:c.71-615A=	NP_001245221.1:n.71-615A=
NM_001258292.2:c.71-615A=	NP_001245221.1:n.71-615A=
NM_001258294.1:c.-13-1129A=	NP_001245223.1:n.-13-1129A=
NM_001258294.2:c.-13-1129A=	NP_001245223.1:n.-13-1129A=
NM_001258295.1:c.-13-1129A=	NP_001245224.1:n.-13-1129A=
NM_001258295.2:c.-13-1129A=	NP_001245224.1:n.-13-1129A=
NM_001258296.1:c.-13-1129A=	NP_001245225.1:n.-13-1129A=
NM_001258296.2:c.-13-1129A=	NP_001245225.1:n.-13-1129A=
NM_001258297.1:c.-13-1129A=	NP_001245226.1:n.-13-1129A=
NM_001258297.2:c.-13-1129A=	NP_001245226.1:n.-13-1129A=
NM_012340.4:c.131-615A=	NP_036472.2:n.131-615A=
NM_173091.3:c.131-615A=	NP_775114.1:n.131-615A=
NM_173091.4:c.131-615A=	NP_775114.1:n.131-615A=
ENST00000371564.7:c.131-615A=	ENSP00000360619.3:n.131-615A=
ENST00000396009.7:c.131-615A=	ENSP00000379330.3:n.131-615A=
ENST00000414705.5:c.71-615A=	ENSP00000396471.1:n.71-615A=
ENST00000609507.1:c.-13-1129A=	ENSP00000477342.1:n.-13-1129A=
ENST00000609943.5:c.71-615A=	ENSP00000477370.1:n.71-615A=
ENST00000610033.5:c.-13-1129A=	ENSP00000477142.1:n.-13-1129A=
XM_011528824.1:c.131-615A=	XP_011527126.1:n.131-615A=
XM_011528824.2:c.131-615A=	XP_011527126.1:n.131-615A=
XM_011528825.1:c.71-615A=	XP_011527127.1:n.71-615A=
XM_011528825.2:c.71-615A=	XP_011527127.1:n.71-615A=
XM_011528826.1:c.-13-1129A=	XP_011527128.1:n.-13-1129A=
XM_011528826.2:c.-13-1129A=	XP_011527128.1:n.-13-1129A=
XM_017027850.1:c.-13-1129A=	XP_016883339.1:n.-13-1129A=
XM_017027851.1:c.131-615A=	XP_016883340.1:n.131-615A=