Canonical Allele Identifier: CA2129438135

Gene: NKX2-1 SFTA3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36517837_36517838delinsAG , CM000676.2:g.36517837_36517838delinsAG	GRCh38
NC_000014.8:g.36987042_36987043delinsAG , CM000676.1:g.36987042_36987043delinsAG	GRCh37
NC_000014.7:g.36056793_36056794delinsAG	NCBI36
NG_013365.1:g.7388_7389delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000522719.4:c.556_557delinsCT (NKX2-1)	ENSP00000429519.4:p.Leu186=
ENST00000354822.7:c.646_647delinsCT (NKX2-1) MANE Select	ENSP00000346879.6:p.Leu216=
ENST00000521945.1:n.54+1630_54+1631delinsCT
ENST00000522719.3:c.*683_*684delinsCT (NKX2-1)	ENSP00000429519.3:n.*683_*684delinsCT
ENST00000546983.2:c.373+1147_373+1148delinsCT	ENSP00000449302.2:n.373+1147_373+1148delinsCT
ENST00000354822.6:c.646_647delinsCT (NKX2-1)	ENSP00000346879.5:p.Leu216=
ENST00000498187.6:c.556_557delinsCT (NKX2-1)	ENSP00000429607.2:p.Leu186=
ENST00000518149.5:c.556_557delinsCT (NKX2-1)	ENSP00000428341.1:p.Leu186=
ENST00000522719.2:c.556_557delinsCT (NKX2-1)	ENSP00000429519.2:p.Leu186=
NM_001079668.2:c.646_647delinsCT (NKX2-1)	NP_001073136.1:p.Leu216=
NM_003317.3:c.556_557delinsCT (NKX2-1)	NP_003308.1:p.Leu186=
NM_001352986.1:c.-283+1630_-283+1631delinsCT (SFTA3)	NP_001339915.1:n.-283+1630_-283+1631delinsCT
NM_001352987.1:c.-237+1630_-237+1631delinsCT (SFTA3)	NP_001339916.1:n.-237+1630_-237+1631delinsCT
NM_001079668.3:c.646_647delinsCT (NKX2-1) MANE Select	NP_001073136.1:p.Leu216=
NM_003317.4:c.556_557delinsCT (NKX2-1)	NP_003308.1:p.Leu186=
NR_161364.1:n.89+1630_89+1631delinsCT (SFTA3)
NR_161365.1:n.89+1630_89+1631delinsCT (SFTA3)