Canonical Allele Identifier: CA1601615629

Gene: NKX2-5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173232493G= , CM000667.2:g.173232493G=	GRCh38
NC_000005.9:g.172659496G= , CM000667.1:g.172659496G=	GRCh37
NC_000005.8:g.172592102G=	NCBI36
NG_013340.1:g.7820C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329198.5:c.*76C= MANE Select	ENSP00000327758.4:n.*76C=
ENST00000329198.4:c.*76C=	ENSP00000327758.4:n.*76C=
NM_001166175.1:c.*1004C=	NP_001159647.1:n.*1004C=
NM_001166176.1:c.*850C=	NP_001159648.1:n.*850C=
NM_004387.3:c.*76C=	NP_004378.1:n.*76C=
NM_004387.4:c.*76C= MANE Select	NP_004378.1:n.*76C=
NM_001166175.2:c.*1004C=	NP_001159647.1:n.*1004C=
NM_001166176.2:c.*850C=	NP_001159648.1:n.*850C=