Canonical Allele Identifier: CA1601615844

Gene: NKX2-5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173232857T= , CM000667.2:g.173232857T=	GRCh38
NC_000005.9:g.172659860T= , CM000667.1:g.172659860T=	GRCh37
NC_000005.8:g.172592466T=	NCBI36
NG_013340.1:g.7456A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329198.5:c.687A= MANE Select	ENSP00000327758.4:p.Pro229=
ENST00000329198.4:c.687A=	ENSP00000327758.4:p.Pro229=
NM_001166175.1:c.*640A=	NP_001159647.1:n.*640A=
NM_001166176.1:c.*486A=	NP_001159648.1:n.*486A=
NM_004387.3:c.687A=	NP_004378.1:p.Pro229=
NM_004387.4:c.687A= MANE Select	NP_004378.1:p.Pro229=
NM_001166175.2:c.*640A=	NP_001159647.1:n.*640A=
NM_001166176.2:c.*486A=	NP_001159648.1:n.*486A=