Canonical Allele Identifier: CA2129438989
Gene: NKX2-1 HGNC NCBI
NKX2-1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36520214C= , CM000676.2:g.36520214C= GRCh38
NC_000014.8:g.36989419C= , CM000676.1:g.36989419C= GRCh37
NC_000014.7:g.36059170C= NCBI36
NG_013365.1:g.5012G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000522719.4:c.-320G= (NKX2-1) ENSP00000429519.4:n.-320G=
ENST00000354822.7:c.-85G= (NKX2-1) MANE Select ENSP00000346879.6:n.-85G=
ENST00000522719.3:c.-85G= (NKX2-1) ENSP00000429519.3:n.-85G=
ENST00000546983.2:c.-14+343G= ENSP00000449302.2:n.-14+343G=
ENST00000354822.6:c.-85G= (NKX2-1) ENSP00000346879.5:n.-85G=
ENST00000518149.5:c.-14+343G= (NKX2-1) ENSP00000428341.1:n.-14+343G=
ENST00000546983.1:c.-85G= (NKX2-1) ENSP00000449302.1:n.-85G=
NM_001079668.2:c.-85G= (NKX2-1) NP_001073136.1:n.-85G=
NR_103710.1:n.402+535C= (NKX2-1-AS1)
NM_001079668.3:c.-85G= (NKX2-1) MANE Select NP_001073136.1:n.-85G=