Canonical Allele Identifier: CA2695205824
Gene: NKX2-5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173234944_173234960del , CM000667.2:g.173234944_173234960del GRCh38
NC_000005.9:g.172661947_172661963del , CM000667.1:g.172661947_172661963del GRCh37
NC_000005.8:g.172594553_172594569del NCBI36
NG_013340.1:g.5355_5371del

Transcript Alleles

HGVS Amino-acid Change
ENST00000329198.5:c.126_142del MANE Select ENSP00000327758.4:p.Pro43GlyfsTer?
ENST00000329198.4:c.126_142del ENSP00000327758.4:p.Pro43GlyfsTer?
ENST00000424406.2:c.126_142del ENSP00000395378.2:p.Pro43GlyfsTer?
ENST00000517440.1:c.126_142del ENSP00000429905.1:p.Pro43GlyfsTer?
ENST00000521848.1:c.126_142del ENSP00000427906.1:p.Pro43GlyfsTer?
NM_001166175.1:c.126_142del NP_001159647.1:p.Pro43GlyfsTer?
NM_001166176.1:c.126_142del NP_001159648.1:p.Pro43GlyfsTer?
NM_004387.3:c.126_142del NP_004378.1:p.Pro43GlyfsTer?
XM_017009071.2:c.126_142del XP_016864560.1:p.Pro43GlyfsTer?
NM_004387.4:c.126_142del MANE Select NP_004378.1:p.Pro43GlyfsTer?
NM_001166175.2:c.126_142del NP_001159647.1:p.Pro43GlyfsTer?
NM_001166176.2:c.126_142del NP_001159648.1:p.Pro43GlyfsTer?