Canonical Allele Identifier: CA7158568
Community Standard Title: NM_001079668.3(NKX2-1):c.190C>A (p.Leu64Ile)
Gene: NKX2-1 HGNC NCBI
SFTA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36519258G>T , CM000676.2:g.36519258G>T GRCh38
NC_000014.8:g.36988463G>T , CM000676.1:g.36988463G>T GRCh37
NC_000014.7:g.36058214G>T NCBI36
NG_013365.1:g.5968C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001079668.3:c.190C>A (NKX2-1) MANE Select NP_001073136.1:p.Leu64Ile
ENST00000354822.7:c.190C>A (NKX2-1) MANE Select ENSP00000346879.6:p.Leu64Ile
NM_001079668.2:c.190C>A (NKX2-1) NP_001073136.1:p.Leu64Ile
NM_001352986.1:c.-283+210C>A (SFTA3) NP_001339915.1:n.-283+210C>A
NM_001352987.1:c.-237+210C>A (SFTA3) NP_001339916.1:n.-237+210C>A
NM_003317.3:c.100C>A (NKX2-1) NP_003308.1:p.Leu34Ile
NM_003317.4:c.100C>A (NKX2-1) NP_003308.1:p.Leu34Ile
NR_161364.1:n.89+210C>A (SFTA3)
NR_161365.1:n.89+210C>A (SFTA3)
ENST00000354822.6:c.190C>A (NKX2-1) ENSP00000346879.5:p.Leu64Ile
ENST00000498187.6:c.100C>A (NKX2-1) ENSP00000429607.2:p.Leu34Ile
ENST00000518149.5:c.100C>A (NKX2-1) ENSP00000428341.1:p.Leu34Ile
ENST00000521945.1:n.54+210C>A
ENST00000522719.2:c.100C>A (NKX2-1) ENSP00000429519.2:p.Leu34Ile
ENST00000522719.3:c.*227C>A (NKX2-1) ENSP00000429519.3:n.*227C>A
ENST00000522719.4:c.100C>A (NKX2-1) ENSP00000429519.4:p.Leu34Ile
ENST00000546983.2:c.100C>A ENSP00000449302.2:p.Leu34Ile