Canonical Allele Identifier: CA962015734
Gene: NKX2-1 HGNC NCBI
SFTA3 HGNC NCBI

Linked Data

dbSNP Id: rs1881133814

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36518110dup , CM000676.2:g.36518110dup GRCh38
NC_000014.8:g.36987315dup , CM000676.1:g.36987315dup GRCh37
NC_000014.7:g.36057066dup NCBI36
NG_013365.1:g.7119dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000522719.4:c.374-87dup (NKX2-1) ENSP00000429519.4:n.374-87dup
ENST00000354822.7:c.464-87dup (NKX2-1) MANE Select ENSP00000346879.6:n.464-87dup
ENST00000521945.1:n.54+1361dup
ENST00000522719.3:c.*501-87dup (NKX2-1) ENSP00000429519.3:n.*501-87dup
ENST00000546983.2:c.373+878dup ENSP00000449302.2:n.373+878dup
ENST00000354822.6:c.464-87dup (NKX2-1) ENSP00000346879.5:n.464-87dup
ENST00000498187.6:c.374-87dup (NKX2-1) ENSP00000429607.2:n.374-87dup
ENST00000518149.5:c.374-87dup (NKX2-1) ENSP00000428341.1:n.374-87dup
ENST00000522719.2:c.374-87dup (NKX2-1) ENSP00000429519.2:n.374-87dup
NM_001079668.2:c.464-87dup (NKX2-1) NP_001073136.1:n.464-87dup
NM_003317.3:c.374-87dup (NKX2-1) NP_003308.1:n.374-87dup
NM_001352986.1:c.-283+1361dup (SFTA3) NP_001339915.1:n.-283+1361dup
NM_001352987.1:c.-237+1361dup (SFTA3) NP_001339916.1:n.-237+1361dup
NM_001079668.3:c.464-87dup (NKX2-1) MANE Select NP_001073136.1:n.464-87dup
NM_003317.4:c.374-87dup (NKX2-1) NP_003308.1:n.374-87dup
NR_161364.1:n.89+1361dup (SFTA3)
NR_161365.1:n.89+1361dup (SFTA3)