Canonical Allele Identifier: CA2129438154

Gene: NKX2-1 SFTA3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36517886G= , CM000676.2:g.36517886G=	GRCh38
NC_000014.8:g.36987091G= , CM000676.1:g.36987091G=	GRCh37
NC_000014.7:g.36056842G=	NCBI36
NG_013365.1:g.7340C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000522719.4:c.508C= (NKX2-1)	ENSP00000429519.4:p.Gln170=
ENST00000354822.7:c.598C= (NKX2-1) MANE Select	ENSP00000346879.6:p.Gln200=
ENST00000521945.1:n.54+1582C=
ENST00000522719.3:c.*635C= (NKX2-1)	ENSP00000429519.3:n.*635C=
ENST00000546983.2:c.373+1099C=	ENSP00000449302.2:n.373+1099C=
ENST00000354822.6:c.598C= (NKX2-1)	ENSP00000346879.5:p.Gln200=
ENST00000498187.6:c.508C= (NKX2-1)	ENSP00000429607.2:p.Gln170=
ENST00000518149.5:c.508C= (NKX2-1)	ENSP00000428341.1:p.Gln170=
ENST00000522719.2:c.508C= (NKX2-1)	ENSP00000429519.2:p.Gln170=
NM_001079668.2:c.598C= (NKX2-1)	NP_001073136.1:p.Gln200=
NM_003317.3:c.508C= (NKX2-1)	NP_003308.1:p.Gln170=
NM_001352986.1:c.-283+1582C= (SFTA3)	NP_001339915.1:n.-283+1582C=
NM_001352987.1:c.-237+1582C= (SFTA3)	NP_001339916.1:n.-237+1582C=
NM_001079668.3:c.598C= (NKX2-1) MANE Select	NP_001073136.1:p.Gln200=
NM_003317.4:c.508C= (NKX2-1)	NP_003308.1:p.Gln170=
NR_161364.1:n.89+1582C= (SFTA3)
NR_161365.1:n.89+1582C= (SFTA3)