Canonical Allele Identifier: CA1601615849

Gene: NKX2-5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173232867T= , CM000667.2:g.173232867T=	GRCh38
NC_000005.9:g.172659870T= , CM000667.1:g.172659870T=	GRCh37
NC_000005.8:g.172592476T=	NCBI36
NG_013340.1:g.7446A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329198.5:c.677A= MANE Select	ENSP00000327758.4:p.Asp226=
ENST00000329198.4:c.677A=	ENSP00000327758.4:p.Asp226=
NM_001166175.1:c.*630A=	NP_001159647.1:n.*630A=
NM_001166176.1:c.*476A=	NP_001159648.1:n.*476A=
NM_004387.3:c.677A=	NP_004378.1:p.Asp226=
NM_004387.4:c.677A= MANE Select	NP_004378.1:p.Asp226=
NM_001166175.2:c.*630A=	NP_001159647.1:n.*630A=
NM_001166176.2:c.*476A=	NP_001159648.1:n.*476A=