Canonical Allele Identifier: CA1601615730
Gene: NKX2-5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173232667C= , CM000667.2:g.173232667C= GRCh38
NC_000005.9:g.172659670C= , CM000667.1:g.172659670C= GRCh37
NC_000005.8:g.172592276C= NCBI36
NG_013340.1:g.7646G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000329198.5:c.877G= MANE Select ENSP00000327758.4:p.Val293=
ENST00000329198.4:c.877G= ENSP00000327758.4:p.Val293=
NM_001166175.1:c.*830G= NP_001159647.1:n.*830G=
NM_001166176.1:c.*676G= NP_001159648.1:n.*676G=
NM_004387.3:c.877G= NP_004378.1:p.Val293=
NM_004387.4:c.877G= MANE Select NP_004378.1:p.Val293=
NM_001166175.2:c.*830G= NP_001159647.1:n.*830G=
NM_001166176.2:c.*676G= NP_001159648.1:n.*676G=