Canonical Allele Identifier: CA362160646
Gene: NKX2-5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173232570T>C , CM000667.2:g.173232570T>C GRCh38
NC_000005.9:g.172659573T>C , CM000667.1:g.172659573T>C GRCh37
NC_000005.8:g.172592179T>C NCBI36
NG_013340.1:g.7743A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000329198.5:c.974A>G MANE Select ENSP00000327758.4:p.Ter325Trp
ENST00000329198.4:c.974A>G ENSP00000327758.4:p.Ter325Trp
NM_001166175.1:c.*927A>G NP_001159647.1:n.*927A>G
NM_001166176.1:c.*773A>G NP_001159648.1:n.*773A>G
NM_004387.3:c.974A>G NP_004378.1:p.Ter325Trp
NM_004387.4:c.974A>G MANE Select NP_004378.1:p.Ter325Trp
NM_001166175.2:c.*927A>G NP_001159647.1:n.*927A>G
NM_001166176.2:c.*773A>G NP_001159648.1:n.*773A>G