Canonical Allele Identifier: CA1601615681
Gene: NKX2-5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173232573C= , CM000667.2:g.173232573C= GRCh38
NC_000005.9:g.172659576C= , CM000667.1:g.172659576C= GRCh37
NC_000005.8:g.172592182C= NCBI36
NG_013340.1:g.7740G=

Transcript Alleles

HGVS Amino-acid change
ENST00000329198.5:c.971G= MANE Select ENSP00000327758.4:p.Trp324=
ENST00000329198.4:c.971G= ENSP00000327758.4:p.Trp324=
NM_001166175.1:c.*924G= NP_001159647.1:n.*924G=
NM_001166176.1:c.*770G= NP_001159648.1:n.*770G=
NM_004387.3:c.971G= NP_004378.1:p.Trp324=
NM_004387.4:c.971G= MANE Select NP_004378.1:p.Trp324=
NM_001166175.2:c.*924G= NP_001159647.1:n.*924G=
NM_001166176.2:c.*770G= NP_001159648.1:n.*770G=