Canonical Allele Identifier: CA258877627

Gene: NKX2-1 SFTA3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36516981del , CM000676.2:g.36516981del	GRCh38
NC_000014.8:g.36986186del , CM000676.1:g.36986186del	GRCh37
NC_000014.7:g.36055937del	NCBI36
NG_013365.1:g.8251del

Transcript Alleles

HGVS	Amino-acid Change
NM_001079668.3:c.*303del (NKX2-1) MANE Select	NP_001073136.1:n.*303del
ENST00000354822.7:c.*303del (NKX2-1) MANE Select	ENSP00000346879.6:n.*303del
NM_001079668.2:c.*303del (NKX2-1)	NP_001073136.1:n.*303del
NM_001352986.1:c.-283+2493del (SFTA3)	NP_001339915.1:n.-283+2493del
NM_001352987.1:c.-237+2493del (SFTA3)	NP_001339916.1:n.-237+2493del
NM_003317.3:c.*303del (NKX2-1)	NP_003308.1:n.*303del
NM_003317.4:c.*303del (NKX2-1)	NP_003308.1:n.*303del
NR_161364.1:n.89+2493del (SFTA3)
NR_161365.1:n.89+2493del (SFTA3)
ENST00000354822.6:c.*303del (NKX2-1)	ENSP00000346879.5:n.*303del
ENST00000498187.6:c.*303del (NKX2-1)	ENSP00000429607.2:n.*303del
ENST00000518149.5:c.*303del (NKX2-1)	ENSP00000428341.1:n.*303del
ENST00000521945.1:n.54+2493del
ENST00000546983.2:c.373+2010del	ENSP00000449302.2:n.373+2010del