Canonical Allele Identifier: CA1601617142

Gene: NKX2-5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173235096A= , CM000667.2:g.173235096A=	GRCh38
NC_000005.9:g.172662099A= , CM000667.1:g.172662099A=	GRCh37
NC_000005.8:g.172594705A=	NCBI36
NG_013340.1:g.5217T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329198.5:c.-13T= MANE Select	ENSP00000327758.4:n.-13T=
ENST00000329198.4:c.-13T=	ENSP00000327758.4:n.-13T=
ENST00000424406.2:c.-13T=	ENSP00000395378.2:n.-13T=
ENST00000517440.1:c.-13T=	ENSP00000429905.1:n.-13T=
ENST00000521848.1:c.-13T=	ENSP00000427906.1:n.-13T=
NM_001166175.1:c.-13T=	NP_001159647.1:n.-13T=
NM_001166176.1:c.-13T=	NP_001159648.1:n.-13T=
NM_004387.3:c.-13T=	NP_004378.1:n.-13T=
XM_017009071.2:c.-13T=	XP_016864560.1:n.-13T=
NM_004387.4:c.-13T= MANE Select	NP_004378.1:n.-13T=
NM_001166175.2:c.-13T=	NP_001159647.1:n.-13T=
NM_001166176.2:c.-13T=	NP_001159648.1:n.-13T=