Canonical Allele Identifier: CA2129438050
Gene: NKX2-1 HGNC NCBI
SFTA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36517644A= , CM000676.2:g.36517644A= GRCh38
NC_000014.8:g.36986849A= , CM000676.1:g.36986849A= GRCh37
NC_000014.7:g.36056600A= NCBI36
NG_013365.1:g.7582T=

Transcript Alleles

HGVS Amino-acid change
ENST00000522719.4:c.750T= (NKX2-1) ENSP00000429519.4:p.Ala250=
ENST00000354822.7:c.840T= (NKX2-1) MANE Select ENSP00000346879.6:p.Ala280=
ENST00000521945.1:n.54+1824T=
ENST00000522719.3:c.*877T= (NKX2-1) ENSP00000429519.3:n.*877T=
ENST00000546983.2:c.373+1341T= ENSP00000449302.2:n.373+1341T=
ENST00000354822.6:c.840T= (NKX2-1) ENSP00000346879.5:p.Ala280=
ENST00000498187.6:c.750T= (NKX2-1) ENSP00000429607.2:p.Ala250=
ENST00000518149.5:c.750T= (NKX2-1) ENSP00000428341.1:p.Ala250=
ENST00000522719.2:c.750T= (NKX2-1) ENSP00000429519.2:p.Ala250=
NM_001079668.2:c.840T= (NKX2-1) NP_001073136.1:p.Ala280=
NM_003317.3:c.750T= (NKX2-1) NP_003308.1:p.Ala250=
NM_001352986.1:c.-283+1824T= (SFTA3) NP_001339915.1:n.-283+1824T=
NM_001352987.1:c.-237+1824T= (SFTA3) NP_001339916.1:n.-237+1824T=
NM_001079668.3:c.840T= (NKX2-1) MANE Select NP_001073136.1:p.Ala280=
NM_003317.4:c.750T= (NKX2-1) NP_003308.1:p.Ala250=
NR_161364.1:n.89+1824T= (SFTA3)
NR_161365.1:n.89+1824T= (SFTA3)