Canonical Allele Identifier: CA1601615940

Gene: NKX2-5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173233010C= , CM000667.2:g.173233010C=	GRCh38
NC_000005.9:g.172660013C= , CM000667.1:g.172660013C=	GRCh37
NC_000005.8:g.172592619C=	NCBI36
NG_013340.1:g.7303G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329198.5:c.534G= MANE Select	ENSP00000327758.4:p.Thr178=
ENST00000329198.4:c.534G=	ENSP00000327758.4:p.Thr178=
ENST00000424406.2:c.*487G=	ENSP00000395378.2:n.*487G=
ENST00000521848.1:c.*333G=	ENSP00000427906.1:n.*333G=
NM_001166175.1:c.*487G=	NP_001159647.1:n.*487G=
NM_001166176.1:c.*333G=	NP_001159648.1:n.*333G=
NM_004387.3:c.534G=	NP_004378.1:p.Thr178=
NM_004387.4:c.534G= MANE Select	NP_004378.1:p.Thr178=
NM_001166175.2:c.*487G=	NP_001159647.1:n.*487G=
NM_001166176.2:c.*333G=	NP_001159648.1:n.*333G=