Canonical Allele Identifier: CA1601615731
Gene: NKX2-5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173232668G= , CM000667.2:g.173232668G= GRCh38
NC_000005.9:g.172659671G= , CM000667.1:g.172659671G= GRCh37
NC_000005.8:g.172592277G= NCBI36
NG_013340.1:g.7645C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000329198.5:c.876C= MANE Select ENSP00000327758.4:p.Phe292=
ENST00000329198.4:c.876C= ENSP00000327758.4:p.Phe292=
NM_001166175.1:c.*829C= NP_001159647.1:n.*829C=
NM_001166176.1:c.*675C= NP_001159648.1:n.*675C=
NM_004387.3:c.876C= NP_004378.1:p.Phe292=
NM_004387.4:c.876C= MANE Select NP_004378.1:p.Phe292=
NM_001166175.2:c.*829C= NP_001159647.1:n.*829C=
NM_001166176.2:c.*675C= NP_001159648.1:n.*675C=