Canonical Allele Identifier: CA1601615697

Gene: NKX2-5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173232602T= , CM000667.2:g.173232602T=	GRCh38
NC_000005.9:g.172659605T= , CM000667.1:g.172659605T=	GRCh37
NC_000005.8:g.172592211T=	NCBI36
NG_013340.1:g.7711A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329198.5:c.942A= MANE Select	ENSP00000327758.4:p.Gly314=
ENST00000329198.4:c.942A=	ENSP00000327758.4:p.Gly314=
NM_001166175.1:c.*895A=	NP_001159647.1:n.*895A=
NM_001166176.1:c.*741A=	NP_001159648.1:n.*741A=
NM_004387.3:c.942A=	NP_004378.1:p.Gly314=
NM_004387.4:c.942A= MANE Select	NP_004378.1:p.Gly314=
NM_001166175.2:c.*895A=	NP_001159647.1:n.*895A=
NM_001166176.2:c.*741A=	NP_001159648.1:n.*741A=