Canonical Allele Identifier: CA389458863

Gene: NKX2-1 SFTA3

Linked Data

• dbSNP Id: rs2139406621
• MyVariant Identifiers: chr14:g.36986818G>C (hg19) ; chr14:g.36517613G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36517613G>C , CM000676.2:g.36517613G>C	GRCh38
NC_000014.8:g.36986818G>C , CM000676.1:g.36986818G>C	GRCh37
NC_000014.7:g.36056569G>C	NCBI36
NG_013365.1:g.7613C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000522719.4:c.781C>G (NKX2-1)	ENSP00000429519.4:p.Pro261Ala
ENST00000354822.7:c.871C>G (NKX2-1) MANE Select	ENSP00000346879.6:p.Pro291Ala
ENST00000521945.1:n.54+1855C>G
ENST00000522719.3:c.*908C>G (NKX2-1)	ENSP00000429519.3:n.*908C>G
ENST00000546983.2:c.373+1372C>G	ENSP00000449302.2:n.373+1372C>G
ENST00000354822.6:c.871C>G (NKX2-1)	ENSP00000346879.5:p.Pro291Ala
ENST00000498187.6:c.781C>G (NKX2-1)	ENSP00000429607.2:p.Pro261Ala
ENST00000518149.5:c.781C>G (NKX2-1)	ENSP00000428341.1:p.Pro261Ala
ENST00000522719.2:c.781C>G (NKX2-1)	ENSP00000429519.2:p.Pro261Ala
NM_001079668.2:c.871C>G (NKX2-1)	NP_001073136.1:p.Pro291Ala
NM_003317.3:c.781C>G (NKX2-1)	NP_003308.1:p.Pro261Ala
NM_001352986.1:c.-283+1855C>G (SFTA3)	NP_001339915.1:n.-283+1855C>G
NM_001352987.1:c.-237+1855C>G (SFTA3)	NP_001339916.1:n.-237+1855C>G
NM_001079668.3:c.871C>G (NKX2-1) MANE Select	NP_001073136.1:p.Pro291Ala
NM_003317.4:c.781C>G (NKX2-1)	NP_003308.1:p.Pro261Ala
NR_161364.1:n.89+1855C>G (SFTA3)
NR_161365.1:n.89+1855C>G (SFTA3)