Canonical Allele Identifier: CA2129438160

Gene: NKX2-1 SFTA3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36517900C= , CM000676.2:g.36517900C=	GRCh38
NC_000014.8:g.36987105C= , CM000676.1:g.36987105C=	GRCh37
NC_000014.7:g.36056856C=	NCBI36
NG_013365.1:g.7326G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000522719.4:c.494G= (NKX2-1)	ENSP00000429519.4:p.Arg165=
ENST00000354822.7:c.584G= (NKX2-1) MANE Select	ENSP00000346879.6:p.Arg195=
ENST00000521945.1:n.54+1568G=
ENST00000522719.3:c.*621G= (NKX2-1)	ENSP00000429519.3:n.*621G=
ENST00000546983.2:c.373+1085G=	ENSP00000449302.2:n.373+1085G=
ENST00000354822.6:c.584G= (NKX2-1)	ENSP00000346879.5:p.Arg195=
ENST00000498187.6:c.494G= (NKX2-1)	ENSP00000429607.2:p.Arg165=
ENST00000518149.5:c.494G= (NKX2-1)	ENSP00000428341.1:p.Arg165=
ENST00000522719.2:c.494G= (NKX2-1)	ENSP00000429519.2:p.Arg165=
NM_001079668.2:c.584G= (NKX2-1)	NP_001073136.1:p.Arg195=
NM_003317.3:c.494G= (NKX2-1)	NP_003308.1:p.Arg165=
NM_001352986.1:c.-283+1568G= (SFTA3)	NP_001339915.1:n.-283+1568G=
NM_001352987.1:c.-237+1568G= (SFTA3)	NP_001339916.1:n.-237+1568G=
NM_001079668.3:c.584G= (NKX2-1) MANE Select	NP_001073136.1:p.Arg195=
NM_003317.4:c.494G= (NKX2-1)	NP_003308.1:p.Arg165=
NR_161364.1:n.89+1568G= (SFTA3)
NR_161365.1:n.89+1568G= (SFTA3)