Canonical Allele Identifier: CA1601615734
Gene: NKX2-5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173232672T= , CM000667.2:g.173232672T= GRCh38
NC_000005.9:g.172659675T= , CM000667.1:g.172659675T= GRCh37
NC_000005.8:g.172592281T= NCBI36
NG_013340.1:g.7641A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000329198.5:c.872A= MANE Select ENSP00000327758.4:p.Asn291=
ENST00000329198.4:c.872A= ENSP00000327758.4:p.Asn291=
NM_001166175.1:c.*825A= NP_001159647.1:n.*825A=
NM_001166176.1:c.*671A= NP_001159648.1:n.*671A=
NM_004387.3:c.872A= NP_004378.1:p.Asn291=
NM_004387.4:c.872A= MANE Select NP_004378.1:p.Asn291=
NM_001166175.2:c.*825A= NP_001159647.1:n.*825A=
NM_001166176.2:c.*671A= NP_001159648.1:n.*671A=