Canonical Allele Identifier: CA1601615677
Gene: NKX2-5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173232560G= , CM000667.2:g.173232560G= GRCh38
NC_000005.9:g.172659563G= , CM000667.1:g.172659563G= GRCh37
NC_000005.8:g.172592169G= NCBI36
NG_013340.1:g.7753C=

Transcript Alleles

HGVS Amino-acid change
ENST00000329198.5:c.*9C= MANE Select ENSP00000327758.4:n.*9C=
ENST00000329198.4:c.*9C= ENSP00000327758.4:n.*9C=
NM_001166175.1:c.*937C= NP_001159647.1:n.*937C=
NM_001166176.1:c.*783C= NP_001159648.1:n.*783C=
NM_004387.3:c.*9C= NP_004378.1:n.*9C=
NM_004387.4:c.*9C= MANE Select NP_004378.1:n.*9C=
NM_001166175.2:c.*937C= NP_001159647.1:n.*937C=
NM_001166176.2:c.*783C= NP_001159648.1:n.*783C=